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1-(3-Chlorophenyl)ethanone → (R)-1-(3-Chlorophenyl)ethanol

HRID 1364427
ノート
印刷プレビュー

反応式

HRID 1364427 の反応式
B.O1CCCC1.[CH3:7][C:8]([C:10]1[CH:15]=[CH:14][CH:13]=[C:12]([Cl:16])[CH:11]=1)=[O:9]>C1(C)C=CC=CC=1.O1CCCC1>[Cl:16][C:12]1[CH:11]=[C:10]([C@H:8]([OH:9])[CH3:7])[CH:15]=[CH:14][CH:13]=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 149331-(3-Chlorophenyl)ethanoneHCID 2723981Borane;tetrahydrofuran2 回

生成物 1

HCID 6950742(R)-1-(3-Chlorophenyl)ethanol収率 78%

試薬・触媒・溶媒 2

HCID 1140Toluene溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of borane-tetrahydrofuran (0.647 mL, 0.647 mmol, Aldrich, 1 M solution in THF) and (S)-MeCBS (0.647 mL, 0.647 mmol, Aldrich, 1M solution in toluene) was added simultaneously a solution of 3-chloroacetophenone (1.00 g, 6.47 mmol) in anhydrous tetrahydrofuran (2.42 mL) and a solution of borane-tetrahydrofuran (3.24 mL, 3.24 mmol, Aldrich, 1 M solution in THF) over 30 min at ambient temperature. After complete addition, the reaction mixture was stirred for 10 min, quenched slowly at 0° C. with methanol (0.94 mL) and then saturated HCl in ether (0.12 mL). After stirring at 0° C. for 5 min and ambient temperature for 30 min, the solution was concentrated in vacuo to an oil. The oil was twice diluted with benzene and concentrated in vacuo, diluted with ether, and concentrated in vacuo to an oil. The oil was purified by flash chromatography (silica gel, 20% EA in hexane) to give (R)-1-(3-chlorophenyl)ethanol as a clear colorless oil (0.784 g, 78%). Optical rotation in CHCl3 at 20° C. at concentration 0.220 was +40.90 (Literature, Bull. Chem. Soc. Jpn. 1996, 69(4), 1079-1085, optical rotation in CHCl3 at 21° C. at concentration 0.220 was +44°).

後処理

  1. additionAfter complete addition
  2. customquenched slowly at 0° C. with methanol (0.94 mL)
  3. stirringAfter stirring at 0° C. for 5 min and ambient temperature for 30 min
  4. concentrationthe solution was concentrated in vacuo to an oil
  5. additionThe oil was twice diluted with benzene
  6. concentrationconcentrated in vacuo
  7. additiondiluted with ether
  8. concentrationconcentrated in vacuo to an oil
  9. customThe oil was purified by flash chromatography (silica gel, 20% EA in hexane)

出典と根拠

ORDレコード
ord-ec0b778c499d43aa81a4d9e4863f9b25
出典データセット
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07888366B2

反応ノート

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