Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287444Generated: November 2, 2026

Water → 2-Benzyl-2-methyl-5-methoxy-6,7-dichloro-1-indanone

https://huagongshe.com/reaction/1287444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
Reactant2-Methyl-5-methoxy-6,7-dichloro-1-indanoneHCID 12395561—
ReactantPotassium tert-butoxideHCID 23665647—
SolventBenzeneHCID 241—
Solventtert-ButanolHCID 6386—
Product2-Benzyl-2-methyl-5-methoxy-6,7-dichloro-1-indanoneHCID 12395566—

Reaction Steps

Potassium tert-butoxide (1.68 g., 0.015 mole) in dry tert-butyl alcohol (40ml.) is added to a refluxing solution of 2-methyl-5-methoxy-6,7-dichloro-1-indanone in benzene (50 ml.). After refluxing for 30 minutes, benzyl bromide (1.72 g., 0.01 mole) in benzene (10 ml.) is added dropwise. After refluxing for an additional 30 minutes the mixture is cooled, water (10 ml.) is added and the mixture is evaporated to dryness. The residue is washed with water and taken up in ether. The ether solution is washed with water and a saturated sodium chloride solution, dried over sodium sulfate and evaporated. The syrupy residue of 2-benzyl-2-methyl-5-methoxy-6,7-dichloro-1-indanone (3 g.) is used directly in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03984465
Source datasetuspto-grants-1976_10
ORD IDord-b66eeadd60e64e0fbd7e48ce5d672d83
Source noteuspto-grants-1976_10