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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1351765Generated: November 1, 2026

Chloromethyl Methyl Ether → 3-(4-Benzyloxy-2-methoxymethoxyphenyl)propionamide

https://huagongshe.com/reaction/1351765

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantSodium hydrideHCID 24758—
Reactant3-(4-Benzyloxy-2-hydroxyphenyl)propionamideHCID 17856263—
SolventDimethylformamideHCID 6228—
Product3-(4-Benzyloxy-2-methoxymethoxyphenyl)propionamideHCID 17856235—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred suspension of 5.64 g of 60% sodium hydride in oil in 628 mL of N,N-dimethylformamide was added 34.8 g of 3-(4-benzyloxy-2-hydroxyphenyl)propionamide under ice-cooling, and the mixture was stirred at 50° C. for 40 minutes. To the reaction mixture was added 12.39 g of chloromethyl methyl ether under ice-cooling, and the mixture was stirred at room temperature for 15 hours. After the reaction mixture was concentrated under reduced pressure to remove the solvent, the residue was poured into a mixture of 500 mL of ethyl acetate, 100 mL of toluene, and 200 mL of water. The organic layer was separated, washed with water, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under reduced pressure to give a colorless solid. The solid was triturated in ethyl acetate-diisopropyl ether to collect by filtration of 35.3 g of 3-(4-benzyloxy-2-methoxymethoxy-phenyl)propionamide as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07217832B2
Source datasetuspto-grants-2007_05
ORD IDord-4bea5bfc294f49bfbfebb00559fe3098
Source noteuspto-grants-2007_05