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HRID 27972作成日:2026年10月25日

Hydrochloric Acid → 4H-1,3-Benzoxazin-4-one, 6-chloro-2-(2-chloropropyl)-2,3-dihydro-3-hydroxy-

https://huagongshe.com/reaction/27972

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Benzamide, 5-chloro-N,2-dihydroxy-HCID 169935—
反応物CrotonaldehydeHCID 447466—
反応物6-chloro-2-methyl-3,3a-dihydro-2H,9H-isoxazolo (3,2-b) (1,3) benzoxazin-9-oneHCID 12365927—
溶媒Acetic AcidHCID 176—
生成物4H-1,3-Benzoxazin-4-one, 6-chloro-2-(2-chloropropyl)-2,3-dihydro-3-hydroxy-HCID 112684—

反応手順

Prior to the present invention, 6-chloro-2-methyl-3,3a-dihydro-2H,9H-isoxazolo (3,2-b) (1,3) benzoxazin-9-one has been prepared by the reaction of 5-chlorosalicylhydroxamic acid (made from 5-chlorosalicylate and hydroxylamine) and crotonaldehyde in the presence of hydrogen chloride and glacial acetic acid to obtain 6-chloro-2-(2-chloropropyl)-2,3-dihydro-3-hydroxy-4H-1,3-benzoxazin-4-one. The latter compound was then cyclized to 7-chloro-2-methyl-3,3a-dihydro-2H,9H-isoxazolo (3,2-b) (1,3) benzoxazin-9-one. Said cyclization can be carried out using organic or inorganic bases in the appropriate solvent. U.S. Pat. No. 3,598,814 discloses and claims 7-chloro-2-methyl-3, 3a-dihydro-2H,9H-isoxazolo (3,2-b) (1,3) benzoxazin-9-one and several methods for its manufacture.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04224443
出典データセットuspto-grants-1980_09
ORD IDord-f831b10a89984c7a966ec6bbcd621d7c
出典メモuspto-grants-1980_09