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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898889Generated: October 26, 2026

Triethylamine → Tert-butyl (4-{2-[(methylsulfonyl)oxy]ethyl}phenoxy)acetate

https://huagongshe.com/reaction/898889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantTert-butyl [4-(2-hydroxyethyl)phenoxy]acetateHCID 23119602—
SolventDichloromethaneHCID 6344—
ProductTert-butyl (4-{2-[(methylsulfonyl)oxy]ethyl}phenoxy)acetateHCID 8660096595.5%

Reaction Conditions

Temperature-10 °C

Reaction Steps

Tert-butyl [4-(2-hydroxyethyl)phenoxy]acetate (6.000 g, 23.781 mmol) and triethylamine (9.9 ml, 71.341 mmol) were dissolved in DCM. The mixture was cooled to −10° C. and methanesulfonyl chloride (2.8 ml, 35.671 mmol) was added dropwise to the mixture. The reaction mixture was allowed to reach room temperature and was stirred for 16 hours. The mixture was diluted with DCM. The organic layer was washed with water, brine and 0.3M KHSO4, dried with MgSO4, and evaporated under reduced pressure. Obtained 7.5 g of light-yellow crystals (yield 95.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07351858B2
Source datasetuspto-grants-2008_04
ORD IDord-645b4593cacc44a79a13e29e22ae538e
Source noteuspto-grants-2008_04