Ethanol → 4-Benzofuranol

HRID 16408

반응식

HRID 16408 반응식
[O:1]1[C:5]2[CH2:6][CH2:7][CH2:8][C:9](=[O:10])[C:4]=2[CH:3]=[CH:2]1.C(O)C>[Pd].C1C2C(CCCC2)CCC1.C=CCCCCCCCCCC>[O:1]1[C:5]2=[CH:6][CH:7]=[CH:8][C:9]([OH:10])=[C:4]2[CH:3]=[CH:2]1

참가 물질

6

반응물 2

HCID 702EthanolHCID 27335414,5,6,7-Tetrahydro-1-benzofuran-4-one

생성물 1

HCID 116079214-Benzofuranol

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 7044Decalin용매HCID 81831-Dodecene용매

반응 조건

온도
80 °C

실험 절차

3.76 g (27.6 mmol) of 6,7-dihydro-1-benzofuran-4(5H)-one (prepared according to Tetrahedron Lett. 1994, 35, 6231) and 10% of palladium on activated carbon in 34 ml of decalin and 6 ml of dodecene are heated in a metal bath at 200° C. overnight. The mixture is cooled to 80° C., ethanol is added and the mixture is filtered off through CELITE (diatomaceous earth). The CELITE (diatomaceous earth) is washed twice with ethanol and the filtrate is concentrated. The residue, which still contains decalin and dodecene, is mixed with petroleum ether and cooled in an ice bath. An oily precipitate forms. The solvent is decanted off and the oil is purified by preparative HPLC.

후처리

  1. filtrationthe mixture is filtered off through CELITE (diatomaceous earth)
  2. washThe CELITE (diatomaceous earth) is washed twice with ethanol
  3. concentrationthe filtrate is concentrated
  4. additionThe residue, which still contains decalin and dodecene, is mixed with petroleum ether
  5. temperaturecooled in an ice bath
  6. customThe solvent is decanted off
  7. customthe oil is purified by preparative HPLC

출처 및 근거

ORD 기록
ord-e53e6d184e694ac9ab2df5d78b9d045c
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07737153B2

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