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Sodium Hydroxide → 2-Sulfanyl-3-[5-(trifluoromethyl)furan-2-yl]prop-2-enoic acid

HRID 67921
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HRID 67921 반응식
[F:1][C:2]([F:17])([F:16])[C:3]1[O:7][C:6]([CH:8]=[C:9]2[S:13]C(=S)N[C:10]2=[O:15])=[CH:5][CH:4]=1.[OH-:18].[Na+]>O>[SH:13][C:9](=[CH:8][C:6]1[O:7][C:3]([C:2]([F:17])([F:16])[F:1])=[CH:4][CH:5]=1)[C:10]([OH:18])=[O:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 538729252-Sulfanylidene-5-{[5-(trifluoromethyl)furan-2-yl]methylidene}-1,3-thiazolidin-4-one

생성물 1

HCID 713702922-Sulfanyl-3-[5-(trifluoromethyl)furan-2-yl]prop-2-enoic acid수율 60%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

1.58 g of the above 5-(5-trifluoromethyl-2-furylmethylene)rhodanine, 23 ml of 1 N sodium hydroxide solution and 25 ml of water are stirred under nitrogen at room temperature for 10 hours. After cooling with an ice bath and acidification with concentrated hydrochloric acid to pH 1.5, the resulting slurry is filtered to yield a slightly brown precipitate which is washed with 50 ml of water by stirring at room temperature under nitrogen and filtered to yield 0.8 g of slightly brown crystals (yield 60%) of α-mercapto-β-(5-trifluoromethyl-2-furyl)acrylic acid. M.P. 158° C.

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후처리

  1. temperatureAfter cooling with an ice bath
  2. filtrationacidification with concentrated hydrochloric acid to pH 1.5, the resulting slurry is filtered
  3. customto yield a slightly brown precipitate which
  4. washis washed with 50 ml of water
  5. filtrationfiltered

출처 및 근거

ORD 기록
ord-2558f552afc342e5b01cb50080fe971e
출처 데이터셋
uspto-grants-1982_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04347255

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