Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1700411Generated: November 2, 2026

Glycolic Acid → Acetyl chloride, [[(1,1-dimethylethyl)dimethylsilyl]oxy]-

https://huagongshe.com/reaction/1700411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlycolic AcidHCID 757—
ReactantOxalyl chlorideHCID 65578—
Reactanttert-Butyldimethylsilyl trifluoromethanesulphonateHCID 123564—
CatalystDimethylformamideHCID 6228—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductAcetyl chloride, [[(1,1-dimethylethyl)dimethylsilyl]oxy]-HCID 1093270037%

Reaction Conditions

Temperature0 °C

Reaction Steps

Glycolic acid (5.0 g, 66 mmol) in pyridine (65 ml) was purged with argon and then treated with tert-butyldimethylsilyl trifluoromethanesulfonate (42 g, 36 ml, 158 mmol) at 0° C., and the mixture was stirred for 2.5 hours. The 2-phase mixture was separated and the upper phase diluted with diethyl ether. This solution was cooled to 0° C., washed briefly with 10% hydrochloric acid, dried (MgSO4) and evaporated to the disilyl material (18 g, 97%). The disilyl material (3.48 g, 12.4 mmol) in dichloromethane (30 ml) at 0° C. was treated with DMF (6 drops) followed by oxalyl chloride (1.84 g, 1.30 ml, 14.50 mmol). After stirring for 3.5 hours, the solution was evaporated and the crude material purified by bulb-to-bulb distillation to afford the title product (60 mbar, 120° C.<T<150° C.) (0.95 g, 37%) contaminated with tert-butyldimethylsiloxane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06350775B1
Source datasetuspto-grants-2002_02
ORD IDord-c401812cefe5415daf29406346374c7d
Source noteuspto-grants-2002_02