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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722483Generated: October 31, 2026

Methanesulfonyl chloride → ethyl (2S)-2-methylsulfonyloxypropanoate

https://huagongshe.com/reaction/1722483

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(L)-ethyl lactateHCID 92831—
SolventTriethylamineHCID 8471—
Productethyl (2S)-2-methylsulfonyloxypropanoateHCID 6364515—

Reaction Steps

An equal molar solution of (S)-ethyl lactate and triethylamine in dry methylene was treated with an equal molar amount of methane sulfonylchloride at 5°-10° C. After the addition was complete, the mixture was filtered to remove triethylamine hydrochloride. The filtrate was then washed with water, dried over MgSO4, and concentrated to give a high yield of ethyl-(S)-2[(methylsulfonyl)oxy]propionate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04855455
Source datasetuspto-grants-1989_08
ORD IDord-e8d93e9e3636409594f61ba603ea88f8
Source noteuspto-grants-1989_08