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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377284Generated: October 31, 2026

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

https://huagongshe.com/reaction/1377284

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 numberUS05663449
Source datasetuspto-grants-1997_09
ORD IDord-fd852f2e851c41ecb5a9f59f495ab7a9
Source noteuspto-grants-1997_09