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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28393Generated: October 25, 2026

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

https://huagongshe.com/reaction/28393

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 numberUS07419974B2
Source datasetuspto-grants-2008_09
ORD IDord-df80d05eca0843ef96b1d0374c0d5837
Source noteuspto-grants-2008_09