Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 894611생성일: 2026년 10월 25일
Potassium Carbonate → alpha-[(5-Acetylamino-4-chloro-2-methoxycarbonylphenyl)oxy]-gamma-butyrolactone
https://huagongshe.com/reaction/894611
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2(3H)-Furanone, 3-bromodihydro- | HCID 95463 | — |
| 반응물 | Methyl 4-acetamido-5-chloro-2-hydroxybenzoate | HCID 13329485 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | alpha-[(5-Acetylamino-4-chloro-2-methoxycarbonylphenyl)oxy]-gamma-butyrolactone | HCID 12925954 | — |
반응 단계
51 g. of Methyl 4-acetylamino-5-chloro-2-hydroxybenzoate and 36.8 g. of anhydrous potassium carbonate were suspended in 350 ml. of N,N-dimethylformamide. To the suspension was added 55 g. of α-bromo-γ-butyrolactone, and the mixture was stirred at 60° C. for 12 hours. The solvent was evaporated off under reduced pressure. The residue was diluted with water and extracted with ethyl acetate. The extract was washed with water, dried and concentrated to remove the solvent. The residue was dissolved in chloroform, and subjected to column chromatography on silica gel, using chloroform as the eluent. The product was recrystallized from methanol. By the above procedure there was obtained α-[(5-acetylamino-4-chloro-2-methoxycarbonylphenyl)oxy]-γ-butyrolactone as pale yellow prisms, m.p. 118°-119° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04284644 |
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| 출처 데이터셋 | uspto-grants-1981_08 |
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| ORD ID | ord-12974d29ce31466e91d9eb068bf367af |
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| 출처 메모 | uspto-grants-1981_08 |
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