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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635784Generated: October 26, 2026

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

https://huagongshe.com/reaction/635784

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

5-Chloro-2-methyl-6-nitrobenzoxazole (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 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 6-amino-5-chloro-2-methylbenzoxazole (1), 22 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06190850B1
Source datasetuspto-grants-2001_02
ORD IDord-8bfb09c16556432eaf7c606f1664e43d
Source noteuspto-grants-2001_02