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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268960Generated: October 30, 2026

Triethylamine → Ethyl 3-(4-benzyloxyphenyl)-2-methanesulfonyloxypropionate

https://huagongshe.com/reaction/1268960

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-(4-Benzyloxyphenyl)-2-hydroxypropionic acid ethyl esterHCID 15186153—
SolventDichloromethaneHCID 6344—
ProductEthyl 3-(4-benzyloxyphenyl)-2-methanesulfonyloxypropionateHCID 18625936—

Reaction Steps

To a solution of ethyl 3-(4-benzyloxyphenyl)lactate (3.32 g) obtained from Reference example 24(a) in anhydrous dichloromethane (30 ml) was added methanesulfonyl chloride (0.94 ml), and then triethylamine (2.47 ml) was added dropwise thereto in an ice bath. The reaction solution was stirred for 3 hours at room temperature and then concentrated under reduced pressure. The residue was partitioned between ethyl acetate and water, and the separated ethyl acetate layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was crystallized from hexane to afford the target compound (3.60 g) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199139B2
Source datasetuspto-grants-2007_04
ORD IDord-e5be4514111348399411fa8d41078fdb
Source noteuspto-grants-2007_04