Sodium Chloride → 7,8-Difluoro-6-[1-(4-propylcyclohexyl)prop-2-ynyloxy]chroman

HRID 1873305노트

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HRID 1873305 반응식
[F:1][C:2]1[C:11]([F:12])=[C:10]2[C:5]([CH2:6][CH2:7][CH2:8][O:9]2)=[CH:4][C:3]=1[OH:13].[CH2:14]([CH:17]1[CH2:22][CH2:21][CH:20]([CH:23](O)[C:24]#[CH:25])[CH2:19][CH2:18]1)[CH2:15][CH3:16].C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CC(OC(/N=N/C(OC(C)C)=O)=O)C.[Cl-].[Na+]>C1COCC1>[F:1][C:2]1[C:11]([F:12])=[C:10]2[C:5]([CH2:6][CH2:7][CH2:8][O:9]2)=[CH:4][C:3]=1[O:13][CH:14]([CH:17]1[CH2:18][CH2:19][CH:20]([CH2:23][CH2:24][CH3:25])[CH2:21][CH2:22]1)[C:15]#[CH:16]

참가 물질

7

실험 절차

5.0 g (26.9 mmol) of 7,8-difluorochroman-6-ol are initially introduced in 65 ml of THF together with 5.33 g (29.6 mmol) of 1-(4-propylcyclohexyl)-prop-2-yn-1-ol and 8.45 g (32.2 mmol) of triphenylphosphine, and 6.79 ml (34.9 mmol) of DIAD are added over the course of 30 min with ice-cooling. After 19 h at RT, semi-saturated sodium chloride solution is added, and the mixture is extracted a number of times with MTBE. The combined organic phases are washed with water and saturated sodium chloride solution, and the solution is dried using sodium sulfate. The residue remaining after removal of the solvents is purified by column chromatography (SiO2, n-pentane:MTBE=2:1), giving 7,8-difluoro-6-[1-(4-propylcyclohexyl)prop-2-ynyloxy]chroman as a pale-brown oil.

후처리

  1. additionare added over the course of 30 min with ice-
  2. temperaturecooling
  3. extractionthe mixture is extracted a number of times with MTBE
  4. washThe combined organic phases are washed with water and saturated sodium chloride solution
  5. customthe solution is dried
  6. customafter removal of the solvents
  7. customis purified by column chromatography (SiO2, n-pentane:MTBE=2:1)

출처 및 근거

ORD 기록
ord-918c2e9f0685481898db33b3d2ac659d
출처 데이터셋
uspto-grants-2012_11
특허 번호
US08303844B2

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