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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065407Generated: October 31, 2026

Water → 3-(Tert-butyldimethylsilyloxy)-2,2-dimethylpropyl methanesulfonate

https://huagongshe.com/reaction/2065407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-{[Tert-butyl(dimethyl)silyl]oxy}-2,2-dimethylpropan-1-olHCID 59012138—
SolventDichloromethaneHCID 6344—
Product3-(Tert-butyldimethylsilyloxy)-2,2-dimethylpropyl methanesulfonateHCID 5743991587%

Reaction Conditions

Temperature0 °C

Reaction Steps

To the solution of 3-(tert-butyl-dimethyl-silanyloxy)-2,2-dimethyl-propan-1-ol (20.4 g, 93 mmol) and triethylamine (26 g, 186 mmol) in dichloromethane (200 mL) at 0° C. was added a dichlormethane solution (20 mL) of methanesulfonyl chloride (Aldrich) (8.69 mL, 112 mmol). The reaction mixture was stirred at 0° C. for 2 h. Water was added. Organic layer was separated, the aqueous layer was extracted with dichlormethane. The combined organic layers were washed with diluted aqueous HCl solution, saturated aqueous NaHCO3 solution, brine, dried over MgSO4, and concentrated to give methanesulfonic acid 3-(tert-butyl-dimethyl-silanyloxy)-2,2-dimethyl-propyl ester as a yellow oil (24 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288431B2
Source datasetuspto-grants-2012_10
ORD IDord-b5daaa25e0a449f6a40d0564b8c7c1cb
Source noteuspto-grants-2012_10