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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 644568Generated: October 30, 2026

3-(t-Butyldimethylsilyloxy)benzaldehyde → 1-[3-(tert-Butyldimethylsilanyloxy)phenyl]propan-1-ol

https://huagongshe.com/reaction/644568

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(t-Butyldimethylsilyloxy)benzaldehydeHCID 11207111—
ReactantHCID 178418443HCID 178418443—
SolventDiethyl EtherHCID 3283—
Product1-[3-(tert-Butyldimethylsilanyloxy)phenyl]propan-1-olHCID 68579551—

Reaction Conditions

Temperature0 °C

Reaction Steps

50 g (0.21 mol) of 3-(tert-butyldimethyl-silanyloxy)benzaldehyde are dissolved in 500 ml of ethyl ether and the mixture is cooled to 0° C. 80 ml (0.24 mol) of a 3.0 M solution of ethylmagnesium bromide are added slowly, and the mixture is stirred for 5 hours. After the usual treatment, the residue obtained is purified by chromatography on a silica column (eluent ethyl acetate 20/hexane 80). A colorless oil is obtained (m=45.8 g; Y=82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700657B2
Source datasetuspto-grants-2010_04
ORD IDord-4b4a01cb649a4491bf392461ba2c5fac
Source noteuspto-grants-2010_04