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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120044Generated: October 31, 2026

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

https://huagongshe.com/reaction/2120044

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 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 numberUS06689549B1
Source datasetuspto-grants-2004_02
ORD IDord-bf5def93c0b74ca1b0e1ff9c6a3129d3
Source noteuspto-grants-2004_02