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HCID 19982273, 화합물 → HCID 53851287, 화합물

HRID 1460699
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HRID 1460699 반응식
[C:1]1([C:7]2[C:11]([C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)=[C:10]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)[N:9]([CH2:24][CH2:25][CH2:26][CH2:27][OH:28])[N:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[Cr](Cl)([O-])(=O)=O.[NH+]1C=CC=CC=1>C(Cl)Cl>[C:1]1([C:7]2[C:11]([C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)=[C:10]([C:18]3[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=3)[N:9]([CH2:24][CH2:25][CH2:26][CH:27]=[O:28])[N:8]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 19982273HCID 19982273, 화합물HCID 178418287HCID 178418287, 화합물

생성물 1

HCID 53851287HCID 53851287, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

3,4,5-Triphenyl-1H-pyrazol-1-butanol (4 g, 10.9 mmol) in dry CH2Cl2 (10 mL) was added to a stirred suspension of pyridinium chlorochromate (7.03 g, 32.6 mmol) in dry CH2Cl2 (370 mL). After 3 hours, the CH2Cl2 was removed in vacuo and the residue diluted with diethyl ether (800 mL) and filtered through diatomateous earth. The organic phase was washed twice with water and once with saturated sodium chloride solution, dried over sodium sulfate and concentrated to furnish 3,4,5-triphenyl-1H-pyrazol-1-butanal as a viscous oil. MS(CI): m/e=367 (MH+)

후처리

  1. customthe CH2Cl2 was removed in vacuo
  2. additionthe residue diluted with diethyl ether (800 mL)
  3. filtrationfiltered through diatomateous earth
  4. washThe organic phase was washed twice with water and once with saturated sodium chloride solution
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-2f03157bd59444789f98140d70f5da0c
출처 데이터셋
uspto-grants-1991_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05071866

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