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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081039Generated: October 31, 2026

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

https://huagongshe.com/reaction/1081039

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 numberUS05583145
Source datasetuspto-grants-1996_12
ORD IDord-50184db6d9354423be4cbe3db0ee4c93
Source noteuspto-grants-1996_12