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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 233041Generated: October 30, 2026

Boron tribromide → HCID 23361289, compound

https://huagongshe.com/reaction/233041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantHCID 23361287HCID 23361287—
SolventChloroformHCID 6212—
ProductHCID 23361289HCID 2336128994%

Reaction Steps

To a solution of 1-benzoyl-2-(3-methoxyphenyl)pyrrolidine (1.0 g) in chloroform (40 ml) was added boron tribromide (99%, 1.0 ml) at -10° C., under nitrogen. The cooling bath was removed after 15 rains, and the reaction mixture was allowed to warm to ambient temperature. Crushed ice was added to the reaction mixture followed by 5:1-chloroform/2-propanol. The layers were separated, and the aqueous phase was extracted with 5:1-chloroform/2-propanol (2 times). The combined organic extracts were washed with saturated sodium bicarbonate solution, dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated. The residue was crystallized from dichloromethane/petroleum ether to give 0.89 g (94%) of product. Recrystallization from 2-propanol/methanol gave the analytical sample, mp 167°-169° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05591856
Source datasetuspto-grants-1997_01
ORD IDord-0e0194b75c324653b833efed2d7c64b7
Source noteuspto-grants-1997_01