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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903887Generated: November 1, 2026

Benzyl Chloride → HCID 13309735, compound

https://huagongshe.com/reaction/1903887

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 numberUS04439225
Source datasetuspto-grants-1984_03
ORD IDord-730becfb76774087b27374fee9c5abf5
Source noteuspto-grants-1984_03