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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1530775Generated: November 2, 2026

5-Chloro-2-methyl-6-nitro-1,3-benzoxazole → 2-Methyl-5-chloro-6-benzoxazolamine

https://huagongshe.com/reaction/1530775

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2-methyl-6-nitro-1,3-benzoxazoleHCID 2764455—
SolventTetrahydrofuranHCID 8028—
Product2-Methyl-5-chloro-6-benzoxazolamineHCID 11275404—

Reaction Steps

Compound (2), (30 g), was dissolved in tetrahydrofuran (150 mL), and Raney-Nickel which had been pre-washed with water (×3) and tetrahydrofuran (×3), was added. The mixture was then hydrogenated at room temperature and 352 kg/dm2 (50 psi) of hydrogen. The reaction is complete in approximately 1.5 hours. After this period, the catalyst is filtered off and the solution concentrated under reduced pressure. The residue is triturated with heptane, cooled and the solid filtered off. Yield 22 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06197492B1
Source datasetuspto-grants-2001_03
ORD IDord-0b03a5b9f7ff4e4abec634ce76a39665
Source noteuspto-grants-2001_03