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Methyl vinyl ketone → Tert-butyl 9-oxo-3-azaspiro[5.5]undec-7-ene-3-carboxylate

HRID 1253716
ノート
印刷プレビュー

反応式

HRID 1253716 の反応式
[OH-].[K+].[CH:3]([CH:5]1[CH2:10][CH2:9][N:8]([C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])[CH2:7][CH2:6]1)=O.[CH:18]([C:20]([CH3:22])=[O:21])=[CH2:19]>C(O)C.C1COCC1>[O:21]=[C:20]1[CH2:18][CH2:19][C:5]2([CH2:10][CH2:9][N:8]([C:11]([O:13][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:12])[CH2:7][CH2:6]2)[CH:3]=[CH:22]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 6570Methyl vinyl ketoneHCID 14797Potassium HydroxideHCID 1514430tert-Butyl 4-formylpiperidine-1-carboxylate

生成物 1

HCID 59311817Tert-butyl 9-oxo-3-azaspiro[5.5]undec-7-ene-3-carboxylate収率 25%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 8028
Tetrahydrofuran
溶媒

反応条件

温度
25 °C

実験手順

3 N KOH in ethanol (7.5 ml) was added to mixture of tert-butyl 4-formylpiperidine-1-carboxylate (60.0 mmol, 1.0 eq.) and methyl vinyl ketone (70.0 mmol, 1.3 eq.) in THF (100 ml) at 0° C. and the mixture was then stirred at 25° C. for 16 h. The solvent was evaporated under reduced pressure and the residue diluted with water (100 ml) and KHSO4 solution at 0° C. The aqueous layer was extracted with MC (2×150 ml). The combined organic layers were washed with brine (100 ml) and dried over sodium sulfate. The solvent was evaporated under reduced pressure and the crude product was purified by silica gel column chromatography eluting with 10-12% ethyl acetate in hexanes to give the desired product as a light brown sticky solid. Yield: 25%

後処理

  1. customThe solvent was evaporated under reduced pressure
  2. additionthe residue diluted with water (100 ml) and KHSO4 solution at 0° C
  3. extractionThe aqueous layer was extracted with MC (2×150 ml)
  4. washThe combined organic layers were washed with brine (100 ml)
  5. dry with materialdried over sodium sulfate
  6. customThe solvent was evaporated under reduced pressure
  7. customthe crude product was purified by silica gel column chromatography
  8. washeluting with 10-12% ethyl acetate in hexanes

出典と根拠

ORDレコード
ord-23a2e45b535147b0aaaf324cc8c6e981
出典データセット
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08455475B2

反応ノート

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