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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006475Generated: October 30, 2026

Chloromethyl Methyl Ether → 3-methoxymethoxy-N-methoxy-N-methylbenzamide

https://huagongshe.com/reaction/1006475

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantSodium hydrideHCID 24758—
Reactant3-hydroxy-N-methoxy-N-methylbenzamideHCID 21865376—
SolventDimethylformamideHCID 6228—
Product3-methoxymethoxy-N-methoxy-N-methylbenzamideHCID 2232196487%

Reaction Conditions

Temperature0 °C

Reaction Steps

69.0 g (380 mmol) of B5 were dissolved in 500 ml of dry dimethylformamide, cooled to 0° C. and 11.5 g (480 mmol) sodium hydride were added and the mixture was allowed to stir for 10 minutes. A solution of 31.2 ml (418 mmol) (chloromethyl)methylether in 100 ml of dry diemthylformamide was added at this temperature over a period of 30 minutes. After stirring at room temperature overnight, the solvent was distilled off and the residue was partitionated between 400 ml of dichloromethane and 100 ml of water. The organic layer was washed with 50 ml of aqueous sodium hydrogen carbonate and two times with water (80 ml each) and finally dried over sodium sulfate. Removing the solvent in vacuo yielded 73.5 g (87%) B6 as a colorless oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06790852B2
Source datasetuspto-grants-2004_09
ORD IDord-9f706f144fc64d6ea349aed4b6b5cd35
Source noteuspto-grants-2004_09