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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1079665Generated: October 30, 2026

1-Bromo-3-chloropropane → 6-(3-Chloropropoxy)-7-methoxy-1-tetralone

https://huagongshe.com/reaction/1079665

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Hydroxy-7-methoxy-1-tetraloneHCID 316839—
SolventAcetoneHCID 180—
Product6-(3-Chloropropoxy)-7-methoxy-1-tetraloneHCID 1044576895.4%

Reaction Steps

A mixture of 6-hydroxy-7-methoxy-1-tetralone (J. Org. Chem., 1985, 50, 4937) (1.5 g, 7.8 mmol), K2CO3 (1.7 g, 12.3 mmol), and acetone (30 ml) was stirred at reflux under nitrogen for 45 minutes. The reaction was cooled to ambient temperature and a solution of 1-bromo-3-chloropropane (1.9 g, 12.1 mmol) dissolved in 8 ml acetone was dripped into the mixture. After total addition, the reaction was heated to reflux and stirred under nitrogen for 21 hours. The reaction was cooled to ambient temperature and filtered. The filter cake was washed well with acetone and the filtrate was concentrated to yield 2.0 g 6-(3-chloropropoxy)-7-methoxy-1-tetralone as an amber oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05580879
Source datasetuspto-grants-1996_12
ORD IDord-a43444df834a40f894b5e1ba89c1dc34
Source noteuspto-grants-1996_12