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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371270Generated: November 1, 2026

Ammonium Chloride → 1-({[tert-Butyl(diphenyl)silyl]oxy}methyl)cyclopropan-1-ol

https://huagongshe.com/reaction/1371270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 2-[[(1,1-dimethylethyl)diphenylsilyl]oxy]acetateHCID 59464758—
ReactantHCID 178418443HCID 178418443—
CatalystTitanium isopropoxideHCID 11026—
SolventTetrahydrofuranHCID 8028—
Product1-({[tert-Butyl(diphenyl)silyl]oxy}methyl)cyclopropan-1-olHCID 52987805100%

Reaction Steps

According to the description in a reference (see: Syn. Lett. 07, 1053–1054, 1999), the title compound was prepared as follows. 12 g (35 mmole) of ethyl 2-{[t-butyl(diphenyl)silyl]oxy}acetate was dissolved in 200 ml of tetrahydrofuran (THF) and 2.2 ml of titaniumtetraisopropoxide was added thereto. To the mixture was slowly added 29.2 ml of ethylmagnesiumbromide (3.0M in THF), and the reaction solution was stirred for 12 hours at room temperature. 20 ml of saturated ammonium chloride was added to stop the reaction. About 150 ml of tetrahydrofuran (THF) used as a solvent was removed by distillation under reduced pressure, and the reaction mixture was extracted twice with 200 ml of ethyl acetate. The ethyl acetate extract was distilled under reduced pressure to give 11.4 g (Yield 100%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157448B2
Source datasetuspto-grants-2007_01
ORD IDord-30b3a42e6e384fc8a0d30b8dc6ff8dba
Source noteuspto-grants-2007_01