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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172961Generated: November 1, 2026

Methanesulfonyl chloride → HCID 86672755, compound

https://huagongshe.com/reaction/2172961

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 stirred 0° C. solution of (2-bromo-pyridin-4-yl)-methanol (3.00 g, 16.0 mmol) and N,N-diisopropylethylamine (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), brine (10 mL), dried over MgSO4, filtered and concentrated to afford crude methanesulfonic acid 2-bromo-pyridin-4-ylmethyl ester, which is used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056858B2
Source datasetuspto-grants-2015_06
ORD IDord-9698243b62334df89aff0a93833b8a8a
Source noteuspto-grants-2015_06