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HRID 1068541作成日:2026年10月27日

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

https://huagongshe.com/reaction/1068541

反応式

関与物質

役割名称HCID仕込み量
反応物5-Chloro-2-methyl-6-nitro-1,3-benzoxazoleHCID 2764455—
溶媒TetrahydrofuranHCID 8028—
生成物2-Methyl-5-chloro-6-benzoxazolamineHCID 11275404—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06251575B1
出典データセットuspto-grants-2001_06
ORD IDord-d85248dc0883441ba2175b05b9e92be2
出典メモuspto-grants-2001_06