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Sodium borohydride → ethyl (2RS,3RS)-3-(3-chlorophenyl)-3-hydroxy-2-[4-(2,2,3,3,3-pentafluoropropyl)benzyl]propionate

HRID 1610754
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HRID 1610754 반응식
[BH4-].[Na+].[Cl:3][C:4]1[CH:5]=[C:6]([C:10](=[O:32])[CH:11]([CH2:17][C:18]2[CH:23]=[CH:22][C:21]([CH2:24][C:25]([F:31])([F:30])[C:26]([F:29])([F:28])[F:27])=[CH:20][CH:19]=2)[C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH:7]=[CH:8][CH:9]=1>CCOCC.[Cl-].[Zn+2].[Cl-]>[Cl:3][C:4]1[CH:5]=[C:6]([CH:10]([OH:32])[CH:11]([CH2:17][C:18]2[CH:23]=[CH:22][C:21]([CH2:24][C:25]([F:30])([F:31])[C:26]([F:28])([F:29])[F:27])=[CH:20][CH:19]=2)[C:12]([O:14][CH2:15][CH3:16])=[O:13])[CH:7]=[CH:8][CH:9]=1
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참가 물질

5

반응물 2

HCID 4311764Sodium borohydrideHCID 22262239Ethyl 3-(3-chlorophenyl)-3-oxo-2-[4-(2,2,3,3,3-pentafluoropropyl)benzyl]propionate

생성물 1

HCID 86593311ethyl (2RS,3RS)-3-(3-chlorophenyl)-3-hydroxy-2-[4-(2,2,3,3,3-pentafluoropropyl)benzyl]propionate수율 89%

시약·촉매·용매 2

HCID 3007855Zincchloride촉매HCID 3283Diethyl Ether
용매
2회

실험 절차

To a suspension (30 ml) of zinc chloride (2.70 g, 19.84 mmol) in ether was added sodium borohydride (1.50 g, 39.68 mmol) at room temperature and the mixture was stirred as it was for 2 hrs. Insoluble material was filtered off. To the filtrate was added a solution of ethyl 3-(3-chlorophenyl)-3-oxo-2-[4-(2,2,3,3,3-pentafluoropropyl)benzyl]propionate (4.45 g, 9.92 mmol) in ether (20 ml), and the mixture was stirred at room temperature for 1 hr. The reaction was quenched with 1N hydrochloric acid. The mixture was diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1, 5:1) to give ethyl (2RS,3RS)-3-(3-chlorophenyl)-3-hydroxy-2-[4-(2,2,3,3,3-pentafluoropropyl)benzyl]propionate (3.95 g, 89%) as a colorless transparent oil.

후처리

  1. filtrationInsoluble material was filtered off
  2. stirringthe mixture was stirred at room temperature for 1 hr
  3. customThe reaction was quenched with 1N hydrochloric acid
  4. additionThe mixture was diluted with ethyl acetate
  5. washwashed with water and saturated brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1, 5:1)

출처 및 근거

ORD 기록
ord-ad1a727f69354d0dadbf3a5c808338eb
출처 데이터셋
uspto-grants-2006_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06982348B2

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