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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237395Generated: November 2, 2026

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

https://huagongshe.com/reaction/2237395

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 numberUS07718646B2
Source datasetuspto-grants-2010_05
ORD IDord-250751aa2a2746758608a7f2152a684c
Source noteuspto-grants-2010_05