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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 417253Generated: October 29, 2026

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

https://huagongshe.com/reaction/417253

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 numberUS08088815B2
Source datasetuspto-grants-2012_01
ORD IDord-c4568b84037b4069b3e98e54a49a15de
Source noteuspto-grants-2012_01