Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 132680Generated: October 27, 2026

Water → 3-Chloro-4-(2-trimethylsilylethoxymethoxy)benzaldehyde

https://huagongshe.com/reaction/132680

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3-Chloro-4-hydroxybenzaldehydeHCID 17022—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
SolventDichloromethaneHCID 6344—
Product3-Chloro-4-(2-trimethylsilylethoxymethoxy)benzaldehydeHCID 86591405—

Reaction Steps

5 g (31.93 mmol) of 5-chloro-4-hydroxybenzaldehyde are dissolved in 300 ml of methylene chloride and 6.7 ml (38.3 mmol) of N,N-diisopropyl-N-ethylamine and 5.9 ml (33.52 mmol) of 2-trimethylsilylethoxymethyl chloride (SEMCl) are added to this at 0° C. The mixture is allowed to return to room temperature and stirred overnight. Water is then added and the mixture is extracted with methylene chloride. The organic phase is dried and the solvent is evaporated off. The product of the title is obtained, which is purified by chromatography on a silica gel column, eluting with a 95/5 and then 9/1 heptane/ethyl acetate mixture.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07388031B2
Source datasetuspto-grants-2008_06
ORD IDord-5495e7bd39314462a56df78bc1cb3c03
Source noteuspto-grants-2008_06