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Methane → 5,6-Dihydroxyindole

HRID 1440377
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인쇄 미리보기

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HRID 1440377 반응식
[N+]([C:4]1[CH:9]=[C:8]([O:10]CC2C=CC=CC=2)[C:7]([O:18]CC2C=CC=CC=2)=[CH:6][C:5]=1[CH2:26][C:27]#[N:28])([O-])=O.C.C(O)C>[Pd].O>[OH:18][C:7]1[CH:6]=[C:5]2[C:4](=[CH:9][C:8]=1[OH:10])[NH:28][CH:27]=[CH:26]2
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 297MethaneHCID 702EthanolHCID 109048382-Nitro-4,5-bis(benzyloxy)phenylacetonitrile

생성물 1

HCID 1146835,6-Dihydroxyindole

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 962Water용매

반응 조건

온도
80 °C

실험 절차

The reaction mixture is prepared in an autoclave by adding 0.04 mole (15 g) of 2-nitro-4,5-dibenzyloxyphenylacetonitrile, 1.5 g of palladium at a concentration of 10% on charcoal and 1.5 g of charcoal to 120 ml of ethanol containing 3 ml of water. These are heated to 80° C. for 2 hours, with stirring, under a hydrogen pressure of 4.105Pa. After cooling, the reaction mixture, which is treated in the same manner as previously, produces 5,6-dihydroxyindole an equivalent yield.

후처리

  1. customThe reaction mixture is prepared in an autoclave
  2. temperatureAfter cooling
  3. additionthe reaction mixture, which is treated in the same manner as previously,

출처 및 근거

ORD 기록
ord-b019b17f92bf4a868470d5ae719198b4
출처 데이터셋
uspto-grants-1996_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05498746

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