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1-Iodopropane → 1-Propylpiperidin-4-ol

HRID 1760968
ノート
印刷プレビュー

反応式

HRID 1760968 の反応式
I[CH2:2][CH2:3][CH3:4].[OH:5][CH:6]1[CH2:11][CH2:10][NH:9][CH2:8][CH2:7]1>CC(C)=O>[OH:5][CH:6]1[CH2:11][CH2:10][N:9]([CH2:2][CH2:3][CH3:4])[CH2:8][CH2:7]1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 336431-IodopropaneHCID 79341Piperidin-4-ol

生成物 1

HCID 136652691-Propylpiperidin-4-ol

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

1-Iodopropane (22 ml) was added dropwise during 15 minutes to a stirred suspension of 4-hydroxypiperidine (20 g) in acetone (250 ml) and the resultant mixture was stirred at ambient temperature for 20 hours. The mixture was evaporated and the residue was partitioned between diethyl ether and 2N aqueous sodium hydroxide solution. The organic phase was washed with brine, dried over magnesium sulphate and evaporated to give 4-hydroxy-N-propylpiperidine as an oil (19.6 g); NMR Spectrum: (DMSOd6) 0.82 (t, 3H), 1.16 (m, 4H), 1.66 (m, 2H), 1.91 (m, 2H), 2.06 (t, 2H), 2.64 (m, 2H), 3.38 (m, 1H), 4.45 (d, 1H); Mass Spectrum: M+H+ 144.

後処理

  1. customThe mixture was evaporated
  2. customthe residue was partitioned between diethyl ether and 2N aqueous sodium hydroxide solution
  3. washThe organic phase was washed with brine
  4. dry with materialdried over magnesium sulphate
  5. customevaporated

出典と根拠

ORDレコード
ord-cc68eb2293d64394bf31adfbe3250c66
出典データセット
uspto-grants-2005_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06846827B1

反応ノート

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