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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699345Generated: October 28, 2026

Pyridine → (R)-2-butanol 4-bromobenzenesulfonate

https://huagongshe.com/reaction/1699345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
Reactantp-Bromobenzenesulfonyl chlorideHCID 7396—
Reactant(-)-2-ButanolHCID 84682—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
Product(R)-2-butanol 4-bromobenzenesulfonateHCID 13172147367%

Reaction Steps

A mixture of 8.2 g of (R)-(−)2-butanol, 31.5 g of 1-bromo-4-benzenesulfonyl chloride, 1.0 g of N,N-dimethyl-4-pyridinamine, 55.5 ml of pyridine and 293 ml of dichloromethane was stirred for 3 days at room temperature. After the addition of water, stirring was continued for 1 hour. The reaction mixture was washed twice with a diluted hydrochloric acid solution and once with water, dried, filtered and evaporated in vacuo. The residue was purified by column chromatography over silica gel using trichloromethane as eluent. The pure fractions were collected and the eluent was evaporated, yielding 11.5 g (35.6%) of (R)-2-butanol 4-bromobenzenesulfonate (ester) (interm. 3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06346518B1
Source datasetuspto-grants-2002_02
ORD IDord-0512fbf6610d414f8e1651e950ebc7f4
Source noteuspto-grants-2002_02