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

HRID 349331
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HRID 349331 반응식
[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]
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참가 물질

6

반응물 4

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

생성물 1

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

시약·촉매·용매 1

HCID 6212Chloroform
용매

실험 절차

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-α-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.

후처리

  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)

출처 및 근거

ORD 기록
ord-8f7a035f97e2409cbd581e2dfa942bd6
출처 데이터셋
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07179820B2

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