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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387249Generated: October 30, 2026

Chloromethyl Methyl Ether → 3-Chloro-4-methoxymethoxy-5-methyl-1-benzoyloxybenzene

https://huagongshe.com/reaction/1387249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Benzoyloxy-2-chloro-6-methylphenolHCID 18504588—
SolventChloroformHCID 6212—
Product3-Chloro-4-methoxymethoxy-5-methyl-1-benzoyloxybenzeneHCID 1850463396%

Reaction Conditions

Temperature0 °C

Reaction Steps

Then, 25 g of 4-benzoyloxy-2-chloro-6-methylphenol was dissolved in 250 ml of chloroform, to which 12 g of chloromethyl methyl ether was added, while stirring at 0° C., and 21 g of N-ethyldiisopropylamine was added dropwise. After heating under reflux for 1 hour, the chloroform layer was washed with water, and concentrated. The residue was subjected to silica gel chromatography, which afforded 27.4 g of 3-chloro-4-methoxymethoxy-5-methyl-1-benzoyloxybenzene (96% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268313B1
Source datasetuspto-grants-2001_07
ORD IDord-3aba41ebb34e40a88affb8866e842043
Source noteuspto-grants-2001_07