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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → HCID 69283695, 화합물

HRID 1293450
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HRID 1293450 반응식
[CH3:1][O:2][C:3]1[C:15]2[NH:14][C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[C:7]=2[CH:6]=[CH:5][CH:4]=1.O.CN([CH:20]=[O:21])C>O=P(Cl)(Cl)Cl>[CH:20]([N:14]1[C:15]2[C:3]([O:2][CH3:1])=[CH:4][CH:5]=[CH:6][C:7]=2[C:8]2[C:13]1=[CH:12][CH:11]=[CH:10][CH:9]=2)=[O:21]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 6228Dimethylformamide2회HCID 107743051-methoxy-9H-carbazole

생성물 1

HCID 69283695HCID 69283695, 화합물수율 96%

시약·촉매·용매 1

HCID 24813Phosphorus oxychloride용매

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온도
0 °C

실험 절차

In a 50 mL round bottomed flask was dissolved POCl3 (0.6 mL, 15.23 mM) in 20 mL of dry DMF. The reaction mixture was stirred at 0° C. in an ice bath. To this was added slowly, 1-methoxy-9H-carbazole (1 g, 5.07 mM) dissolved in 30 mL of dry DMF. The reaction mixture was stirred for 2 hrs. Water was added to the reaction mixture and the precipitated product was filtered off. The residue was dissolved in EtOAc and was washed with brine and dried over anh. Na2SO4. Ethyl acetate was then evaporated to obtain the desired product as a white fluffy solid with a yield of 96% (1.1 g); mp 161-163° C.

후처리

  1. additionTo this was added slowly
  2. stirringThe reaction mixture was stirred for 2 hrs
  3. filtrationthe precipitated product was filtered off
  4. dissolutionThe residue was dissolved in EtOAc
  5. washwas washed with brine
  6. dry with materialdried over anh. Na2SO4
  7. customEthyl acetate was then evaporated

출처 및 근거

ORD 기록
ord-7557f0b913a1412abfd3ce55d2f414b8
출처 데이터셋
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07238725B2

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