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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015583Generated: October 30, 2026

Vinyl benzoate → Acetate

https://huagongshe.com/reaction/1015583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantVinyl benzoateHCID 13037—
Solventtert-Butyl methyl etherHCID 15413—
ProductAcetateHCID 175—
ProductFormateHCID 283—
ProductButyrateHCID 104775—

Reaction Steps

A mixture consisting of Intermediate B (80 mg, 0.23 mmol), vinyl ester (0.4 ml), tert.-butyl methylether (18 ml), and lipase enzyme (1.0 g) was gently shaken at room temperature. Benzylic formate, acetate, and n-butyrate were prepared from the corresponding vinyl ester donors using SAM I lipase (Amano Pharmaceutical Co.). Benzoylation was achieved with vinyl benzoate in the presence of Lipozym IM 20 (Novo Nordisk), whereas pivalates and isobutyrates were obtained from the corresponding vinyl esters under catalysis of Novozym SP 435 (Novo Nordisk). Tlc analysis indicated after 2-24 hrs complete disappearence of the starting material (Rf=0.45 (3)). The mixture was filtered and then evaporated under high vacuum (<40° C.) to give the carboxylic acid (R1—CO2H) salts of the respective benzylic monoesters as colourless to light yellow oils.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985772B2
Source datasetuspto-grants-2011_07
ORD IDord-909f3ebd2ef84c69854e6ab5410289e8
Source noteuspto-grants-2011_07