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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-[4-(methylthio)phenyl]-4-oxobutanoic acid → 116174-33-5

HRID 985775
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인쇄 미리보기

반응식

HRID 985775 반응식
[CH3:1][S:2][C:3]1[CH:8]=[CH:7][C:6]([C:9](=O)[CH2:10][CH2:11][C:12]([OH:14])=[O:13])=[CH:5][CH:4]=1.[H-].C([SiH](CC)CC)C>FC(F)(F)C(O)=O>[CH3:1][S:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:9][CH2:10][CH2:11][C:12]([OH:14])=[O:13])=[CH:7][CH:8]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 20637154-[4-(methylthio)phenyl]-4-oxobutanoic acidHCID 131724811HCID 131724811, 화합물

생성물 1

HCID 21916663116174-33-5

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

반응 조건

온도
0 °C

실험 절차

In a 500 ml round-bottomed flask, 0.088 mol of the compound obtained in Step A is dissolved in 0.881 ml of trifluoroacetic acid. The solution is cooled to 0° C. with the aid of an ice bath and 0.220 ml of triethylsilane hydride is added with the aid of a dropping funnel. The reaction mixture is stirred for 18 hours at ambient temperature and is then hydrolysed. The precipitate formed is filtered off under suction, is washed with water and with cyclohexane and is then dissolved in ethyl acetate. The organic phase is dried over MgSO4 and evaporated to obtain the title product in the form of a white solid.

후처리

  1. customThe precipitate formed
  2. filtrationis filtered off under suction
  3. washis washed with water and with cyclohexane
  4. dissolutionis then dissolved in ethyl acetate
  5. dry with materialThe organic phase is dried over MgSO4
  6. customevaporated

출처 및 근거

ORD 기록
ord-be3d8eb2fae044a7ade46c3559bcb064
출처 데이터셋
uspto-grants-2005_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06872851B1

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