Ethyl Acetate → Ethyl 4-(m-methoxyphenyl)-3-phenyl-3-hydroxybutyrate

HRID 2085055

反応式

HRID 2085055 の反応式
C[Si](C)(C)N[Si](C)(C)C.[Li].[C:11]([O:14][CH2:15][CH3:16])(=[O:13])[CH3:12].[C:17]1([C:23]([CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[C:28]([O:32][CH3:33])[CH:27]=2)=[O:24])[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>C1COCC1>[CH3:33][O:32][C:28]1[CH:27]=[C:26]([CH2:25][C:23]([C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)([OH:24])[CH2:12][C:11]([O:14][CH2:15][CH3:16])=[O:13])[CH:31]=[CH:30][CH:29]=1

参加物

5

反応物 3

HCID 8857Ethyl AcetateHCID 27596142-(3-Methoxyphenyl)-1-phenylethan-1-oneHCID 57426343Lithium bis(trimethylsilyl)amide

生成物 1

HCID 22602685Ethyl 4-(m-methoxyphenyl)-3-phenyl-3-hydroxybutyrate収率 86%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-78 °C

実験手順

Lithium hexamethyidisilazane (88.5 mL, 88.5 mmol) was added to THF (150 mL) at −78° C. After 15 minutes, ethyl acetate (7.79 g, 88.5 mmol) was added over 10 minutes and stirred at −78° C. for 30 minutes. The m-methoxybenzyl phenyl ketone in (10.0 g, 44.25 mmol) THF (100 mL) was added over 15 minutes and kept at that temperature for 3 hours. The reaction mixture was quenched at that temperature with saturated ammonium chloride (15 mL). The reaction mixture was diluted with ether (200 mL) and the organic layer was washed with brine, (100 mL), dried and concentrated to afford the desired product (12 g, 86% yield). NMR was consistent with the desired structure.

後処理

  1. waitkept at that temperature for 3 hours
  2. customThe reaction mixture was quenched at that temperature with saturated ammonium chloride (15 mL)
  3. additionThe reaction mixture was diluted with ether (200 mL)
  4. washthe organic layer was washed with brine, (100 mL)
  5. customdried
  6. concentrationconcentrated

出典と根拠

ORDレコード
ord-0d7cb346805c40b583610cf6d62715e4
出典データセット
uspto-grants-2004_04
特許番号
US06720315B2

関連ノート

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