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Trifluoroacetic acid → (R)-6-(1-ethoxyethoxymethyl)-piperidin-2-one

HRID 2052934
ノート
印刷プレビュー

反応式

HRID 2052934 の反応式
[CH:1]([O:3][CH2:4][CH3:5])=[CH2:2].FC(F)(F)C(O)=O.[OH:13][CH2:14][C@@H:15]1[NH:20][C:19](=[O:21])[CH2:18][CH2:17][CH2:16]1.C([O-])(O)=O.[Na+]>C(Cl)(Cl)Cl>[CH2:1]([O:3][CH:4]([O:13][CH2:14][C@@H:15]1[NH:20][C:19](=[O:21])[CH2:18][CH2:17][CH2:16]1)[CH3:5])[CH3:2]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 6422Trifluoroacetic acidHCID 8023Ethyl vinyl etherHCID 516892Sodium BicarbonateHCID 10887932(6R)-6-(hydroxymethyl)piperidin-2-one

生成物 1

HCID 58961293(R)-6-(1-ethoxyethoxymethyl)-piperidin-2-one収率 80.7%

試薬・触媒・溶媒 1

HCID 6212Chloroform
溶媒

実験手順

Ethyl vinyl ether (1.68 mL, 17.5 mmol) and trifluoroacetic acid (0.1 mL) were added sequentially to a solution of (R)-6-hydroxymethylpiperidin-2-one (prepared from D-□-aminoadipic acid according to Huang, et al., Synth. Commun. 1989, 19, 3485-3496, 1.62 g, 12.5 mmol) in CHCl3 (10 mL) at rt. The reaction mixture was stirred at rt for 18 h, then saturated aqueous NaHCO3 (100 mL) was added and the mixture was extracted with CH2Cl2 (3×75 mL). The combined organic phase was dried (Na2SO4), filtered and concentrated in vacuo. Purification of the residue by flash column chromatography on silica gel (CH2Cl2→4% MeOH/CH2Cl2, gradient) afforded 2.03 g (80%) of (R)-6-(1-ethoxyethoxymethyl)-piperidin-2-one.

後処理

  1. extractionthe mixture was extracted with CH2Cl2 (3×75 mL)
  2. dry with materialThe combined organic phase was dried (Na2SO4)
  3. filtrationfiltered
  4. concentrationconcentrated in vacuo
  5. customPurification of the residue by flash column chromatography on silica gel (CH2Cl2→4% MeOH/CH2Cl2, gradient)

出典と根拠

ORDレコード
ord-21cfb9b7ebf548cd83e0803ded673b34
出典データセット
uspto-grants-2008_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07326716B2

反応ノート

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