Hydrochloric Acid → 4-(4-Butoxy-2,3-difluorophenyl)-4'-propylbicyclohexyl-4-ol

HRID 2220576노트

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HRID 2220576 반응식
[CH2:1]([O:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([F:12])[C:7]=1[F:13])[CH2:2][CH2:3][CH3:4].[Li]CCCC.[CH2:19]([CH:22]1[CH2:27][CH2:26][CH:25]([CH:28]2[CH2:33][CH2:32][C:31](=[O:34])[CH2:30][CH2:29]2)[CH2:24][CH2:23]1)[CH2:20][CH3:21].Cl>C1COCC1>[CH2:1]([O:5][C:6]1[CH:11]=[CH:10][C:9]([C:31]2([OH:34])[CH2:30][CH2:29][CH:28]([CH:25]3[CH2:26][CH2:27][CH:22]([CH2:19][CH2:20][CH3:21])[CH2:23][CH2:24]3)[CH2:33][CH2:32]2)=[C:8]([F:12])[C:7]=1[F:13])[CH2:2][CH2:3][CH3:4]

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 27829391-Butoxy-2,3-DifluorobenzeneHCID 4354185[1,1'-Bicyclohexyl]-4-one,4'-propyl-,HCID 178418339Butyllithium

생성물 1

HCID 589918854-(4-Butoxy-2,3-difluorophenyl)-4'-propylbicyclohexyl-4-ol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

31.0 g (0.17 mol) of 1-butoxy-2,3-difluorobenzene are initially introduced in 200 ml of THF, and 100 ml (0.16 mol) of n-BuLi (15% soln. in hexane) are added at −70° C. After 2 h at this temperature, a solution of 35.6 g (0.16 mol) of 4′-propylbicyclohexyl-4-one in 200 ml of THF is metered in, and the batch is stirred for 2.5 h. The reaction mixture is hydrolysed with ice-cooling and acidified using 2 N HCl. The solution is extracted with MTBE, and the combined organic phases are washed with sat. sodium chloride solution and dried using sodium sulfate. The solution is concentrated to dryness, and the crude product (66.3 g of yellow solid) is used directly for the following reaction.

후처리

  1. temperaturecooling
  2. extractionThe solution is extracted with MTBE
  3. washthe combined organic phases are washed with sat. sodium chloride solution
  4. customdried
  5. concentrationThe solution is concentrated to dryness
  6. customthe crude product (66.3 g of yellow solid) is used directly for the following reaction

출처 및 근거

ORD 기록
ord-16d624de9cda4318a0367a9c6529983c
출처 데이터셋
uspto-grants-2008_08
특허 번호
US07417157B2

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