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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259405Generated: November 2, 2026

1-Bromo-3-chloropropane → 6-Chloro-3-(3-chloropropyl)-2(3H)-benzothiazolone

https://huagongshe.com/reaction/2259405

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-3-chloropropaneHCID 8006—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 53400706HCID 53400706—
SolventAcetoneHCID 180—
Product6-Chloro-3-(3-chloropropyl)-2(3H)-benzothiazoloneHCID 1900350893.5%

Reaction Steps

A solution of 6-chloro-benzothiazolone (VIII) (55.7 g, 0.3 mol), K2CO3 (62.1 g, 0.45 mol) and 1-bromo-3-chloropropane (IX) (71 g, 0.45 mol) in acetone (600 ml) was refluxed for 16 hours. After cooling, the inorganic substance was filtered off and washed dichloromethane. The filtrate and washings were combined and evaporated in vacuo. The residue was washed with hexane and recrystallized from dichloromethane to obtain compound (X) (73.5 g, yield=93.4%) as colorless needle-shaped crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05473066
Source datasetuspto-grants-1995_12
ORD IDord-fc6c6655846d4acfaf8a67555ceb05d1
Source noteuspto-grants-1995_12