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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1423065Generated: November 1, 2026

Methanesulfonyl chloride → HCID 86672755, compound

https://huagongshe.com/reaction/1423065

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant(2-Bromopyridin-4-yl)methanolHCID 14512957—
SolventDichloromethaneHCID 6344—
ProductHCID 86672755HCID 86672755—

Reaction Steps

To a chilled (0° C.) solution of (2-bromopyridin-4-yl)-methanol (3.00 g, 16.0 mmol) and DIPEA (8.3 mL, 48 mmol) in dichloromethane (30 mL) is added methanesulfonyl chloride (1.30 mL, 16.8 mmol). The resulting mixture is warmed to room temperature. After 1 hour, the mixture is diluted with dichloromethane (20 mL) and washed with saturated aqueous ammonium chloride (3×10 mL), saturated aqueous sodium bicarbonate (10 mL) and brine (10 mL), dried over MgSO4, filtered and concentrated to afford crude methanesulfonic acid 2-bromopyridin-4-ylmethyl ester, which is used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927550B2
Source datasetuspto-grants-2015_01
ORD IDord-a69dc61edfa6485bbaf7074045cc9895
Source noteuspto-grants-2015_01