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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 628385Generated: October 29, 2026

Triethylamine → 3-({[Tert-butyl(diphenyl)silyl]oxy}methyl)-5-chlorobenzyl methanesulfonate

https://huagongshe.com/reaction/628385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant[3-({[tert-Butyl(diphenyl)silyl]oxy}methyl)-5-chlorophenyl]methanolHCID 123144720—
SolventDichloromethaneHCID 6344—
Product3-({[Tert-butyl(diphenyl)silyl]oxy}methyl)-5-chlorobenzyl methanesulfonateHCID 123575839—

Reaction Steps

Triethylamine (7.8 mL, 56 mmol) and methanesulfonyl chloride (2.9 mL, 37 mmol) were added to a solution of [3-({[tert-butyl(diphenyl)silyl]oxy}methyl)-5-chlorophenyl]methanol (7.65 g, 18.6 mmol, from Step 2) in DCM (50 mL) at 0° C. The cooling bath was removed and after reaction mixture warmed to room temperature, the reaction mixture was diluted with DCM and washed with water. The aqueous layer was extracted with two further portions of DCM. The combined organic extracts were washed with brine, dried over sodium sulfate, filtered and concentrated. The product was purified by flash chromatography, eluting with a gradient from 0-40% EtOAc/hexanes. Yield: (6.8 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309246B2
Source datasetuspto-grants-2016_04
ORD IDord-a5269669f92c494eb4c83c6f2b3b2297
Source noteuspto-grants-2016_04