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Methanol → 1-(4-Methoxybenzyl)piperidine-4-carboxaldehyde

HRID 424617
ノート
印刷プレビュー

反応式

HRID 424617 の反応式
[H-].C([Al+]CC(C)C)C(C)C.[CH3:11][O:12][C:13]1[CH:29]=[CH:28][C:16]([CH2:17][N:18]2[CH2:23][CH2:22][CH:21]([C:24](OC)=[O:25])[CH2:20][CH2:19]2)=[CH:15][CH:14]=1.CO.[Cl-].[Na+]>C1(C)C=CC=CC=1>[CH3:11][O:12][C:13]1[CH:14]=[CH:15][C:16]([CH2:17][N:18]2[CH2:23][CH2:22][CH:21]([CH:24]=[O:25])[CH2:20][CH2:19]2)=[CH:28][CH:29]=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 887MethanolHCID 5234Sodium ChlorideHCID 21225700DiisobutylaluminumhydrideHCID 60704011HCID 60704011、化合物

生成物 1

HCID 178939301-(4-Methoxybenzyl)piperidine-4-carboxaldehyde

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒2 回

実験手順

A 1.5 M solution of diisobutylaluminium hydride in toluene (3.12 ml, 4.68 mmol) was added dropwise to a solution of methyl 1-(4-methoxybenzyl)piperidine-4-carboxylate (1.23 g, 4.68 mmol) in toluene (30 ml) under argon at −78° C. in the course of 30 min and the mixture was then stirred at this temperature for 30 min. Thereafter, methanol (15 ml) was added dropwise such that the internal temperature remained at −78° C., before the mixture was then slowly warmed to room temperature. Saturated sodium chloride solution (20 ml) was added to the reaction mixture and the suspension was filtered through sea sand. The organic phase was dried with sodium sulfate and concentrated i. vac. The residue was purified by flash chromatography with cyclohexane/ethyl acetate (1:3).

後処理

  1. customremained at −78° C., before the mixture
  2. filtrationthe suspension was filtered through sea sand
  3. dry with materialThe organic phase was dried with sodium sulfate
  4. concentrationconcentrated i
  5. customThe residue was purified by flash chromatography with cyclohexane/ethyl acetate (1:3)

出典と根拠

ORDレコード
ord-bb27e75eb7a647f39d22d5a4043b3d73
出典データセット
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08106055B2

反応ノート

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