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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
ノート
印刷プレビュー

反応式

HRID 1610754 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 3007855Zincchloride触媒HCID 3283Diethyl Ether
溶媒
2 回

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-ad1a727f69354d0dadbf3a5c808338eb
出典データセット
uspto-grants-2006_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06982348B2

反応ノート

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