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Isobutyraldehyde → HCID 11300027、化合物

HRID 131189
ノート
印刷プレビュー

反応式

HRID 131189 の反応式
[CH2:1]([N:8]1[CH2:13][CH2:12][O:11][CH2:10][C:9]1=[O:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([N-]C(C)C)(C)C.[Li+].[CH:23](=[O:27])[CH:24]([CH3:26])[CH3:25]>O1CCCC1>[CH2:1]([N:8]1[CH2:13][CH2:12][O:11][CH:10]([CH:23]([OH:27])[CH:24]([CH3:26])[CH3:25])[C:9]1=[O:14])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=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 3

HCID 6561IsobutyraldehydeHCID 2724682Lithium diisopropylamideHCID 122940874-Benzylmorpholin-3-one

生成物 1

HCID 11300027HCID 11300027、化合物

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

実験手順

To a stirred solution of 2 (5.05 g, 26.4 mmol) in tetrahydrofuran (25 ml) at −78° C. under nitrogen was added lithium diisopropylamide (14.5 ml of a 2M solution, 29.0 mmol) dropwise over 40 minutes. The reaction mixture was stirred at the same temperature over 30 minutes after which time a solution of isobutyraldehyde (2.63 ml, 29.0 mmol) in tetrahydrofuran (15 ml) was added dropwise over 30 minutes. After one hour, the reaction mixture was allowed to warm to room temperature and quenched by addition of saturated ammonium chloride solution. Extraction with dichloromethane and drying over magnesium sulphate gave 53 as a mixture of diastereomers. Upon concentration in vacuo one diastereomer precipitated as a white solid (53a: 0.99 g). The remaining mother liquors were purified by column chromatography (30% ethyl acetate in hexane [v/v]) to give 53 (2.06 g). MW 263.34; C15H21NO3; LCMS (6 min method): m/z 286 [M+Na]+; RT=2.748.

後処理

  1. additionwas added dropwise over 30 minutes
  2. customquenched by addition of saturated ammonium chloride solution
  3. extractionExtraction with dichloromethane
  4. dry with materialdrying over magnesium sulphate

出典と根拠

ORDレコード
ord-d9b56de4fdf94651b96639cdaf7e1b1b
出典データセット
uspto-grants-2008_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07384941B2

反応ノート

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