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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906436Generated: October 25, 2026

Sodium hydride → (1-(((tert-Butyldimethylsilyl)oxy)methyl)cyclopropyl)methanol

https://huagongshe.com/reaction/906436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant1,1-Bis(hydroxymethyl)cyclopropaneHCID 4101437—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product(1-(((tert-Butyldimethylsilyl)oxy)methyl)cyclopropyl)methanolHCID 5900090470.2%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of cyclopropane-1,1-diyldimethanol (3.7 g) dissolved in ethylene glycol dimethyl ether (50 mL) was treated with 60% sodium hydride (1.449 g) at 0° C. under nitrogen. The resulting mixture was stirred at 20° C. for 1 h, treated with tert-butylchlorodimethylsilane (5.46 g) and stirred at room temperature overnight. The reaction mixture was diluted with water (250 mL), and extracted with ethyl acetate (2×250 mL). The organic was dried (MgSO4), filtered and evaporated to afford crude product. The crude product was purified (SiO2 chromatography, elution 100% DCM). Pure fractions were evaporated to dryness to afford the subtitle compound (5.50 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012980B2
Source datasetuspto-grants-2011_09
ORD IDord-3550cdff5c8e47f3abd24d89c79ace22
Source noteuspto-grants-2011_09