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Hydrochloric Acid → 2,8a-dibenzyl-1,2,3,4,8,8a-hexahydroisoquinolin-6(7H)-one

HRID 1042322
ノート
印刷プレビュー

反応式

HRID 1042322 の反応式
[CH2:1]([N:8]1[CH2:13][CH2:12][C:11](=O)[CH:10]([CH2:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C[O-].[Na+].[CH3:25][C:26]([CH:28]=[CH2:29])=[O:27].Cl>CO>[CH2:1]([N:8]1[CH2:13][CH2:12][C:11]2[C:10]([CH2:15][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)([CH2:29][CH2:28][C:26](=[O:27])[CH:25]=2)[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1
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 313Hydrochloric AcidHCID 6570Methyl vinyl ketoneHCID 10942334Sodium MethoxideHCID 230036591,3-Dibenzylpiperidin-4-one

生成物 1

HCID 444429102,8a-dibenzyl-1,2,3,4,8,8a-hexahydroisoquinolin-6(7H)-one

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

1,3-Dibenzylpiperidin-4-one (3, R1B=H, Z=benzyl) (3.98 g, 13.96 mmol) was added to a solution of sodium methoxide (0.83 g, 15.36 mmol) in 80 mL of methanol and stirred at ambient temperature for 45 min. The contents were cooled to 0° C. and methylvinyl ketone (1.74 mL, 20.94 mmol) was added over 30 min. The contents were allowed to warm to ambient temperature and stir for 18 h. Concentrated HCl (1.55 mL) was added, the contents were stirred for a further 5 min and the solvents were evaporated to give a brown oil which was triturated in diethyl ether to give the title compound, 1.90 g. LC-MS: RT=2.26 min. (M+H)+ 332.

後処理

  1. temperatureThe contents were cooled to 0° C.
  2. temperatureto warm to ambient temperature
  3. stirringstir for 18 h
  4. stirringthe contents were stirred for a further 5 min
  5. customthe solvents were evaporated
  6. customto give a brown oil which
  7. customwas triturated in diethyl ether

出典と根拠

ORDレコード
ord-78622167dabc420eae04c95e2ab3355b
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08557839B2

反応ノート

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