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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

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium HydroxideHCID 14923—
반응물5-[[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-3-[2-(acetyloxy)ethyl]-4-thiazolidinoneHCID 53867199—
용매AcetonitrileHCID 6342—
생성물5-[[3,5-Bis(1,1-dimethylethyl)-4-hydroxyphenyl]methylene]-3-(2-hydroxyethyl)-4-thiazolidinoneHCID 5450750246.7%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05731336
출처 데이터셋uspto-grants-1998_03
ORD IDord-dab83e5f8e4f453e9acc6425fd301ce5
출처 메모uspto-grants-1998_03