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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394566Generated: October 30, 2026

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

https://huagongshe.com/reaction/2394566

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 numberUS05811430
Source datasetuspto-grants-1998_09
ORD IDord-26b363f8448d41d6aa398f32394fccd3
Source noteuspto-grants-1998_09