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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558331Generated: October 24, 2026

Water → Ethyl 3-chloromethyl-4-methoxybenzoate

https://huagongshe.com/en/reaction/558331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantTin tetrachlorideHCID 24287—
ReactantEthyl anisateHCID 60979—
SolventDichloromethaneHCID 6344—
ProductEthyl 3-chloromethyl-4-methoxybenzoateHCID 2314140360%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 4-methoxybenzoate (28.0 mL) and 26.0 mL of methoxymethyl chloride were dissolved in 500 mL of dichloromethane, and the solution was cooled to 0° C. To this solution, 10.0 mL of tin (IV) chloride was added dropwise over 15 minutes, and then the mixture was stirred for 5 hours. The reaction mixture was poured into 1 L of water, and the organic layer was separated, whereafter the aqueous layer was extracted twice with dichloromethane. The organic layer was washed with a saturated aqueous solution of sodium chloride, and dried over anhydrous sodium sulfate. The anhydrous sodium sulfate was separated by filtration, and washed with dichloromethane. The filtrate and the washings were combined, and dichloromethane was distilled off under reduced pressure. The resulting residue was recrystallized from a mixture of n-hexane and ethyl acetate. The resulting crystals were separated by filtration, then washed with n-hexane, and dried under reduced pressure to obtain 23.8 g (60%) of ethyl 3-chloromethyl-4-methoxybenzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063046B2
Source datasetuspto-grants-2011_11
ORD IDord-3ea8928d88a246369e576bc214f5aa0f
Source noteuspto-grants-2011_11