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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412664Generated: November 2, 2026

Benzyl Chloride → HCID 13309735, compound

https://huagongshe.com/reaction/2412664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantHCID 12867349HCID 12867349—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventSodium HydroxideHCID 14798—
ProductHCID 13309735HCID 1330973580.2%

Reaction Steps

A mixture of 3,4-dihydro-2,6-dimethyl-2H-pyran-2-methanol (5.8 g) and benzyl chloride (5.2 g) in 50% aqueous sodium hydroxide (16 g) and 10 ml methylene chloride was treated with 0.7 g tetrabutylammonium hydrogen sulfate. After stirring vigorously for 21 hours at room temperature, the mixture was diluted with more methylene chloride and water to facilitate phase separation. The organic phase was separated, washed with water, dried over potassium carbonate and concentrated. Distillation gave 7.6 g colorless liquid with bp 101°-102° C. (0.02 torr).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04493936
Source datasetuspto-grants-1985_01
ORD IDord-27cd4da8e77b4349b8d98c66b6ec22cd
Source noteuspto-grants-1985_01