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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173181Generated: October 31, 2026

Triethylamine → Tert-butyl 3-bromo-5-{[(methylsulfonyl)oxy]methyl}benzoate

https://huagongshe.com/reaction/2173181

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantTert-butyl 3-bromo-5-(hydroxymethyl)benzoateHCID 58096191—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 3-bromo-5-{[(methylsulfonyl)oxy]methyl}benzoateHCID 86693004—

Reaction Steps

To a DCM (20 mL) solution of tert-butyl 3-bromo-5-(hydroxymethyl)benzoate (1.2 g, 4.2 mmol) was added methanesulfonyl chloride (0.62 g, 5.5 mmol) and triethylamine (1.2 mL, 8.4 mmol) at 0° C. The mixture was allowed to stir for 16 hours. TLC showed clean conversion. The reaction was diluted with DCM (100 mL), washed with 0.1 N HCl (100 mL) and brine, dried over sodium sulfate, and concentrated to afford tert-butyl 3-bromo-5-{[(methylsulfonyl)oxy]methyl}benzoate as a light yellow oil, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056859B2
Source datasetuspto-grants-2015_06
ORD IDord-88a5b421f62d42f59566b270abf9c679
Source noteuspto-grants-2015_06