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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625888Generated: November 3, 2026

5-Bromo-2-chloro-1-(4-methoxycarbonyl-5-oxazolylmethyl)benzene → 1-(3-Amino-2-oxopropyl)-5-bromo-2-chlorobenzene-hydro-chloride

https://huagongshe.com/reaction/1625888

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-chloro-1-(4-methoxycarbonyl-5-oxazolylmethyl)benzeneHCID 66608182—
SolventHydrochloric AcidHCID 313—
Product1-(3-Amino-2-oxopropyl)-5-bromo-2-chlorobenzene-hydro-chlorideHCID 66608810279.2%

Reaction Steps

The above 5-bromo-2-chloro-1-(4-methoxycarbonyl-5-oxazolylmethyl)benzene (1.37 g) was heated under reflux in 6N aqueous hydrochloric acid solution (20 ml) overnight. The solvent was evaporated under reduced pressure, and the residue was dissolved in methanol, and treated with carbon powder. The carbon powder was filtered off, and the filtrate was evaporated under reduced pressure to give crude 1-(3-amino-2-oxopropyl)-5-bromo-2-chlorobenzene.hydrochloride (1.73 g) as a pale brown solid, which was used in the subsequent step without further purification. APCI-Mass m/Z 262/264 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785403B2
Source datasetuspto-grants-2014_07
ORD IDord-59cf1ac6004347c18b62a7ad287af3e1
Source noteuspto-grants-2014_07