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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416077Generated: October 25, 2026

Benzyl Chloride → 2-Benzyloxy-6-chlorotoluene

https://huagongshe.com/reaction/1416077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Chloro-o-cresolHCID 14856—
SolventMethyl Ethyl KetoneHCID 6569—
Product2-Benzyloxy-6-chlorotolueneHCID 1174653488.3%

Reaction Steps

A mixture of 143 g (1.0 mol) of 3-chloro-2-methylphenol, 139 g (1.1 mol) of benzyl chloride, 276 g (2.0 mol) of potassium carbonate and 680 g of methyl ethyl ketone (MEK) is heated under reflux with stirring. After 8 hours, a further 25 g (0.18 mol) of potassium carbonate are added and the mixture is then heated under reflux for a further 8 hours. The batch is filtered and the filter cake is washed with MEK. After working up by distillation, 206 g of 2-benzyloxy-6-chlorotoluene (b.p. 161 ° C., 3 mbar) are obtained as a pale yellow liquid in 99.6% purity (surface area % according to GC). This corresponds to a yield of 88.3% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05910605
Source datasetuspto-grants-1999_06
ORD IDord-fedab3ab2c1942d7bfcf8c467207f665
Source noteuspto-grants-1999_06