Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2944생성일: 2026년 10월 24일
Ammonium Hydroxide → 5-[[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-3-(2-hydroxyethyl)-4-thiazolidinone
https://huagongshe.com/ko/reaction/2944
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Ammonium Hydroxide | HCID 14923 | — |
| 반응물 | 5-[[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-3-[2-(acetyloxy)ethyl]-4-thiazolidinone | HCID 53867199 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 5-[[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-3-(2-hydroxyethyl)-4-thiazolidinone | HCID 54507502 | 46.7% |
반응 단계
A solution of 85.2 g of 5-[[3,5-bis(1,1-dimethylethyl) -4-hydroxyphenyl]methylene]-3-[2-(acetyloxy)ethyl]-4-thiazolidinone from Example 26 in 1.5 l of acetonitrile was treated with 1 liter of concentrated ammonium hydroxide. The reaction mixture was allowed to stand for approximately 90 hours at room temperature. The solution was concentrated in vacuo and 500 ml of ethyl acetate were added, with the pH adjusted to 3.0 with concentrated hydrochloric acid. The layers were separated and the aqueous layer extracted with 250 ml of ethyl acetate. The combined organic layers were washed with 250 ml of a saturated sodium chloride solution and concentrated in vacuo. The residue was crystallized from 95 ml of hexane and 70 ml of ethyl acetate to provide 35.68 g of the desired subtitled intermediate, m.p. 131°-135° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05731336 |
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| 출처 데이터셋 | uspto-grants-1998_03 |
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| ORD ID | ord-dab83e5f8e4f453e9acc6425fd301ce5 |
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| 출처 메모 | uspto-grants-1998_03 |
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