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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1940259Generated: October 26, 2026

Triethylamine → Methyl toluenesulfonyloxyacetate

https://huagongshe.com/reaction/1940259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanto-Toluenesulfonyl chlorideHCID 8623—
ReactantMethyl GlycolateHCID 66774—
SolventDichloromethaneHCID 6344—
ProductMethyl toluenesulfonyloxyacetateHCID 8675174598.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

18 g (0.2 mol) of methyl hydroxyacetate and 20.2 g (0.2 mol) of triethylamine are first introduced into 300 ml of dichloromethane at 0° C. 41.9 g (0.22 mol) of toluenesulfonyl chloride are then added at this temperature in small portions. Stirring of the batch at 0° C. is continued overnight. Ice water is added, the phases are separated, and the aqueous phase is extracted three times with dichloromethane. The combined organic phases are washed once with water, dried, and the solvent is removed on a rotary evaporator. 48 g (98% of theory) of methyl toluenesulfonyloxyacetate having a GC content of 96% are isolated as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05698735
Source datasetuspto-grants-1997_12
ORD IDord-49cbc3da55944ccc97d427074c032aa5
Source noteuspto-grants-1997_12