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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27972생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/27972

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Benzamide, 5-chloro-N,2-dihydroxy-HCID 169935—
반응물CrotonaldehydeHCID 447466—
반응물6-chloro-2-methyl-3,3a-dihydro-2H,9H-isoxazolo (3,2-b) (1,3) benzoxazin-9-oneHCID 12365927—
용매Acetic AcidHCID 176—
생성물4H-1,3-Benzoxazin-4-one, 6-chloro-2-(2-chloropropyl)-2,3-dihydro-3-hydroxy-HCID 112684—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04224443
출처 데이터셋uspto-grants-1980_09
ORD IDord-f831b10a89984c7a966ec6bbcd621d7c
출처 메모uspto-grants-1980_09