// Workers AI · dad joke modeWhat did the ortho ester say? I'm bonded to you.
In organic chemistry, an ortho ester is a functional group containing three alkoxy groups attached to one carbon atom, i.e. with the general formula RC(OR')3. Orthoesters may be considered as products of exhaustive alkylation of unstable orthocarboxylic acids and it is from these that the name 'ortho ester' is derived. An example is ethyl orthoacetate, CH3C(OCH2CH3)3, more correctly known as 1,1,1-triethoxyethane.[1] In total synthesis, bicyclic OBO ortho esters are used as protecting groups for carboxylic acids and esters.
Synthesis
[edit]Ortho esters are traditionally, but inefficiently[2] prepared through the Pinner reaction of nitriles and alcohols in the presence of one equivalent of hydrogen chloride. The reaction requires anhydrous conditions,[1] and ideally a nonpolar solvent.[3]: 6 It begins with formation of imido ester hydrochloride:
- RCN + R′OH + HCl → [RC(OR′)=NH2]+Cl−
Upon standing in the presence of excess alcohol, this intermediate converts to the ortho ester:[citation needed]
- [RC(OR′)=NH2]+Cl− + 2 R′OH → RC(OR′)3 + NH4Cl
A major side-reaction converts the alcohol to the corresponding alkyl chloride.[2]
Acid chlorides can also drive the reaction from the corresponding amide, e.g.:[4]: 154
- HCONH2 + BzCl → HC(OBz)NH2Cl
- HC(OBz)NH2Cl + ROH → HC(OR)3 + NH4Cl + BzOH.
Although a less common method, ortho esters were first produced by reaction of 1,1,1-trichloroalkanes with sodium alkoxide:[1]
- RCCl3 + 3 NaOR′ → RC(OR′)3 + 3 NaCl
Compounds with an adjacent hydrogen atom on R tend to undergo elimination instead.[3]: 12 Traditional esters can be converted to α,α‑dichloro ethers with phosphorus pentachloride. The resulting halogenated compounds undergo ether synthesis like the trichloroalkanes.[4]: 162
Carboxylic acids naturally form a trithio ortho ester when heated with a mercaptan of appropriate stoichiometry.[5] The resulting compound undergoes transesterification to a traditional orthoester in the presence of zinc chloride.[4]: 156
Transesterification from a cheaper ortho ester is also possible;[4] but performs best with unstabilized (electron-poorer) ortho esters. Stabilized ortho-esters tend to collapse to the corresponding non-ortho ester.[2]: 555–556
Reactions
[edit]Hydrolysis
[edit]Ortho esters are readily hydrolyzed in mild aqueous acid to form esters:
- RC(OR′)3 + H2O → RCO2R′ + 2 R′OH
For example, trimethyl orthoformate CH(OCH3)3 may be hydrolyzed (under acidic conditions) to methyl formate and methanol;[6] and may be further hydrolyzed (under alkaline conditions) to salts of formic acid and methanol.[7]
Adamantane-structured orthoesters, formally derived from all-cis-1,3,5-trihydroxycyclohexane, hydrolyze particularly slowly, for which reason they have been used as protecting groups.[8]
Johnson–Claisen rearrangement
[edit]The Johnson–Claisen rearrangement is the reaction of an allylic alcohol with an ortho ester containing a deprotonatable alpha carbon (e.g. triethyl orthoacetate) to give a γ,δ-unsaturated ester.[9]
Bodroux–Chichibabin aldehyde synthesis
[edit]In the Bodroux–Chichibabin aldehyde synthesis an ortho ester reacts with a Grignard reagent to form an aldehyde; this is an example of a formylation reaction.
Examples
[edit]
Examples of orthoesters include the reagents trimethyl orthoformate and triethylorthoacetate. Another example is the bicyclic OBO protecting group (4-methyl-2,6,7-trioxa-bicyclo[2.2.2]octan-1-yl) which is formed by the action of (3-methyloxetan-3-yl)methanol on activated carboxylic acids in the presence of Lewis acids such as BF3. The group is base stable and can be cleaved in two steps under mild conditions. Mildly acidic hydrolysis yields the ester of tris(hydroxymethyl)ethane which is then cleaved using e.g. an aqueous carbonate solution.[10]
The threefold symmetry of the cyclohexanehexol isomer scyllo-inositol (scyllitol) yields the triply-bridged orthoformate esters scyllitol orthoformate with an adamantane-like skeleton, and scyllitol bis-orthoformate with a diamantane-like skeleton.[11]
Hygromycin B, an antibiotic, is one of several naturally occurring ortho esters.
See also
[edit]- Acetal, C(OR)2R2
- Orthocarbonate, C(OR)4.
References
[edit]- 1 2 3 E. H. Cordes (1969). "Ortho Esters". In Saul Patai (ed.). Carboxylic Acids and Esters. PATAI'S Chemistry of Functional Groups. pp. 623–667. doi:10.1002/9780470771099.ch13. ISBN 9780470771099.
- 1 2 3 Hünig, S. (1964). "The modes of reaction of ambident cations". Angewandte Chemie. 3 (8) (International ed.): 552. doi:10.1002/anie.196405481.
- 1 2 DeWolfe, Robert H. (1970). Carboxylic Ortho Acid Derivatives. Organic Chemistry. Vol. 14. New York, NY: Academic Press. LCCN 70-84226.
- 1 2 3 4 DeWolfe, Robert H. (March 1974). "Synthesis of carboxylic or carbonic ortho esters". Synthesis (3): 153–172. doi:10.1055/s-1974-23268.
- ↑ Houben, J. "Über die Condensation von Mercaptanen mit Ameisensäure zu Orthotrithio-ameisensäureestern" [On the condensation of mercaptans with formic acid unto formic acid trithio ortho esters]. Berichte der Deutschen Chemischen Gesellschaft (in German). 45: 2942–2946. doi:10.1002/cber.19120450319 – via the Internet Archive.
- ↑ Clayden, Jonathan; Greeves, Nick; Warren, Stuart; Wothers, Peter (2001). Organic Chemistry (1st ed.). Oxford University Press. p. 345. ISBN 978-0-19-850346-0.
- ↑ United States Patent Application 20070049501, Saini; Rajesh K.; and Savery; Karen, March 1, 2007
- ↑ Fort, Raymond C. (1976). Adamantane. Studies in Organic Chemistry. Vol. 5. New York, NY: Marcel Dekker. pp. 294–295.
- ↑ Johnson, William Summer.; Werthemann, Lucius.; Bartlett, William R.; Brocksom, Timothy J.; Li, Tsung-Tee.; Faulkner, D. John.; Petersen, Michael R. (February 1970). "Simple stereoselective version of the Claisen rearrangement leading to trans-trisubstituted olefinic bonds. Synthesis of squalene". Journal of the American Chemical Society. 92 (3): 741–743. doi:10.1021/ja00706a074.
- ↑ Kocieński, Philip J. (2005). Protecting Groups (3rd ed.). Stuttgart: Thieme. p. 101. ISBN 978-3-13-135603-1.
- ↑ Lee, Hyo Won; Kishi, Yoshito (November 1985). "Synthesis of mono- and unsymmetrical bis-orthoesters of scyllo-inositol". The Journal of Organic Chemistry. 50 (22): 4402–4404. doi:10.1021/jo00222a046.