Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 35555생성일: 2026년 10월 24일
Thioglycolic Acid → alpha-(4-chlorophenyl)-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)-3-methoxybenzeneacetonitrile
https://huagongshe.com/ko/reaction/35555
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Thioglycolic Acid | HCID 1133 | — |
| 반응물 | 2-[4-[(4-Chlorophenyl)cyanomethyl]3-methoxyphenyl]-2,3,4,5-tetrahydro-3,5-dioxo-1,2,4-triazine-6-carboxylic acid | HCID 23035195 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | alpha-(4-chlorophenyl)-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)-3-methoxybenzeneacetonitrile | HCID 23035191 | — |
반응 단계
A mixture of 4.2 parts of 2-[4-[(4-chlorophenyl)cyanomethyl]-3-methoxyphenyl]-2,3,4,5-tetrahydro-3,5-dioxo-1,2,4-triazine-6-carboxylic acid and 13 parts of 2-mercaptoacetic acid is stirred and heated for 2 hours at 175° C. After cooling, 150 parts of water are added. The aqueous phase is decanted and the remaining oil is stirred in water. The whole is treated with sodium hydrogen carbonate. The product is extracted with a mixture of trichloromethane and methanol (90:10 by volume). The extract is dried, filtered and evaporated. The residue is purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (97:3 by volume) as eluent. The pure fractions are collected and the eluent is evaporated in vacuo. The residue is crystallized from 8 parts of acetonitrile. The product is filtered off, washed with 2,2'-oxybispropane and dried, yielding α-(4-chlorophenyl)-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)-3-methoxybenzeneacetonitrile (intermediate 2).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04767760 |
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| 출처 데이터셋 | uspto-grants-1988_08 |
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| ORD ID | ord-4b03e10db0a0402f84e62c9d91cfd833 |
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| 출처 메모 | uspto-grants-1988_08 |
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