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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2166333Generated: November 2, 2026

Chloroform → HCID 14577239, compound

https://huagongshe.com/reaction/2166333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantThionyl bromideHCID 68176—
ReactantHCID 23039520HCID 23039520—
SolventWaterHCID 962—
ProductHCID 14577239HCID 1457723944.2%

Reaction Steps

To 170 ml of chloroform were added 9.9 g of 4-chloro-5-(4'-chlorobenzyloxy)-2-(3'-hydroxypropyl)-3(2H)-pyridazinone (0.03 mol) and slowly added 9.4 g of thionyl bromide (0.045 mol) under stirring for about 2 hours at -5° to 5° C. After reaction, the resulting solution was added little by little with water and the chloroform layer was separated. The layer was washed with water and then with aqueous solution of 5% sodium hydrogen carbonate, and further washed with saturated saline and dried over anhydrous sodium sulfate and freed of solvent by distillation under reduced pressure. The solid product thus obtained was recrystallized from a mixed solvent of n-hexane-benzene to give 5.2 g of 2-(3'-bromopropyl)-4-chloro-5-(4'-chlorobenzyloxy)-3(2H)-pyridazinone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04945091
Source datasetuspto-grants-1990_07
ORD IDord-f1e41692634c44f6bf32bd2dbb7a4b55
Source noteuspto-grants-1990_07