4-Bromopyridine → 8-Bromo-10,11-dihydro-10-(4-pyridinyl)dibenz[b,f]oxepin-10-ol

HRID 1982158노트

반응식

HRID 1982158 반응식
Br[C:2]1[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=1.C([Li])CCC.[Li]C1C=CN=CC=1.[Br:20][C:21]1[CH:22]=[CH:23][C:24]2[O:30][C:29]3[CH:31]=[CH:32][CH:33]=[CH:34][C:28]=3[CH2:27][C:26](=[O:35])[C:25]=2[CH:36]=1>CCOCC.CCCCCC>[Br:20][C:21]1[CH:22]=[CH:23][C:24]2[O:30][C:29]3[CH:31]=[CH:32][CH:33]=[CH:34][C:28]=3[CH2:27][C:26]([C:2]3[CH:7]=[CH:6][N:5]=[CH:4][CH:3]=3)([OH:35])[C:25]=2[CH:36]=1

참가 물질

7

실험 절차

Under an argon atmosphere, a solution of 4-bromopyridine (16.6 g) in anhydrous ether (90 ml) previously cooled to -40°, was transferred slowly via a cannular to a stirred solution of n-butyl lithium in hexane (1.55M; 68 ml) cooled to -78°. The mixture was stirred at -78° for 20 minutes and the resulting 4-lithiopyridine was transferred to a chilled (-78°) stirred suspension of 8-bromodibenz[b,f]oxepin-10(11H)-one (15 g) in anhydrous ether (100 ml). The reaction was stirred at -78° for 30 minutes, then the cooling bath was removed and the mixture was treated with 100 ml of water and allowed to warm to room temperature. The solids were filtered off, washed with water and dried to give 5.0 g of 8-bromo-10,11-dihydro-10-(4-pyridinyl)dibenz[b,f]oxepin-10-ol. The mother liquor was worked up and a total of 9.4 grams of the starting ketone 8-bromodibenz[b,f]oxepin-10(11H)-one were recovered.

후처리

  1. temperaturecooled to -78°
  2. temperaturea chilled (-78°)
  3. stirringstirred
  4. stirringThe reaction was stirred at -78° for 30 minutes
  5. customthe cooling bath was removed
  6. additionthe mixture was treated with 100 ml of water
  7. filtrationThe solids were filtered off
  8. washwashed with water
  9. customdried

출처 및 근거

ORD 기록
ord-8537de479302484e9b21610f229c08e7
출처 데이터셋
uspto-grants-1986_06
특허 번호
US04595689

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