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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trifluoroacetic acid → HCID 58432983, 화합물

HRID 388421
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HRID 388421 반응식
C([O:5][C:6]([C:8]1[C:9]([C:19]2[CH:24]=[CH:23][C:22]([Cl:25])=[CH:21][CH:20]=2)=[N:10][S:11][C:12]=1[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:7])(C)(C)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[Cl:25][C:22]1[CH:21]=[CH:20][C:19]([C:9]2[C:8]([C:6]([OH:7])=[O:5])=[C:12]([C:13]3[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=3)[S:11][N:10]=2)=[CH:24][CH:23]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 58432990HCID 58432990, 화합물

생성물 1

HCID 58432983HCID 58432983, 화합물수율 92.7%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a solution of 11 (2.35 g) in CH2Cl2 (25 ml) is added 25 ml of TFA and the mixture is stirred at room temperature for 24 h. The mixture is then concentrated and the residue is dissolved in ether (250 ml). Water (225 ml) is added followed by 1N NaOH (25 ml). After washing and separation, the basic water layer is extracted once more with ether. The water layer is acidified with conc. HCl and the precipitated product is extracted with ether (2×150 ml). The combined organic layers are washed with brine, dried and concentrated. 1.85 g of 12 is obtained as a cream colored solid.

후처리

  1. concentrationThe mixture is then concentrated
  2. dissolutionthe residue is dissolved in ether (250 ml)
  3. additionWater (225 ml) is added
  4. washAfter washing
  5. customseparation
  6. extractionthe basic water layer is extracted once more with ether
  7. extractionthe precipitated product is extracted with ether (2×150 ml)
  8. washThe combined organic layers are washed with brine
  9. customdried
  10. concentrationconcentrated

출처 및 근거

ORD 기록
ord-a6dfdb0745614ff3ad276c70ec4a0de3
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08377953B2

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