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Dimethylformamide → HCID 19102568, 화합물

HRID 1198546
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HRID 1198546 반응식
[H-].[Na+].C[C:4](P(OC)(O)=O)([C:6]([O-:8])=[O:7])[CH3:5].[CH2:14]([O:21][C:22]1[C:30]2[NH:29][CH:28]=[CH:27][C:26]=2[C:25](C=O)=[CH:24][CH:23]=1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.[CH3:33]N(C)C=O>O1CCCC1>[CH2:14]([O:21][C:22]1[CH:23]=[CH:24][C:25](/[CH:5]=[CH:4]/[C:6]([O:8][CH3:33])=[O:7])=[C:26]2[C:30]=1[NH:29][CH:28]=[CH:27]2)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 24758Sodium hydrideHCID 132434867-(Benzyloxy)-1H-indole-4-carbaldehydeHCID 53413272Trimethylphosphonoacetate

생성물 1

HCID 19102568HCID 19102568, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

60% Sodium hydride dispersion (0.10 g, 2.5 mmol) was added to a stirred solution of trimethylphosphonoacetate (0.41 ml, 2.5 mmol) in tetrahydrofuran (10 ml). The pale suspension was stirred for 1 hour at room temperature then a solution of 7-benzyloxyindole-4-carboxaldehyde (0.63 g, 2.5 mmol) in tetrahydrofuran (5 ml) was added followed by dimethylformamide (5 ml) to give a clear solution. The solution was stirred for 1 hour at room temperature then evaporated under high vacuum. The residue in ethyl acetate was washed with dilute hydrochloric acid dried and concentrated to give pale solid.

후처리

  1. customto give a clear solution
  2. stirringThe solution was stirred for 1 hour at room temperature
  3. customthen evaporated under high vacuum
  4. washThe residue in ethyl acetate was washed with dilute hydrochloric acid
  5. customdried
  6. concentrationconcentrated
  7. customto give pale solid

출처 및 근거

ORD 기록
ord-a22637df0ac647a783a8837d65e55557
출처 데이터셋
uspto-grants-1994_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05281593

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