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Water → 4-(Azetidin-1-yl)piperidine dihydrochloride

HRID 492847
ノート
印刷プレビュー

反応式

HRID 492847 の反応式
[ClH:1].Cl.[N:3]1([CH:7]2[CH2:12][CH2:11][N:10](CC3C=CC=CC=3)[CH2:9][CH2:8]2)[CH2:6][CH2:5][CH2:4]1.O>CC(O)C.[C].[Pd]>[ClH:1].[ClH:1].[N:3]1([CH:7]2[CH2:12][CH2:11][NH:10][CH2:9][CH2:8]2)[CH2:6][CH2:5][CH2:4]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 962WaterHCID 231533984-(Azetidin-1-yl)-1-benzylpiperidine dihydrochloride

生成物 1

HCID 231531084-(Azetidin-1-yl)piperidine dihydrochloride収率 185.1%

試薬・触媒・溶媒 2

HCID 178418390HCID 178418390、化合物触媒HCID 3776Isopropanol溶媒

実験手順

After adding 10% palladium-carbon (600 mg) to a solution of the crude 4-(azetidin-1-yl)-1-benzylpiperidine dihydrochloride (6.55 g) in 2-propanol (50 ml)-water (50 ml), the mixture was stirred for 23 hours at room temperature under a hydrogen atmosphere. The catalyst was filtered and washed with 2-propanol, and then the filtrate was concentrated. Ethanol (10 ml)-hexane (50 ml) was added to the residue to produce suspended precipitate. It was then filtered and washed with 10 ml of ethanol. The filtered precipitate was subjected to aeration drying to provide the title compound (4.26 g) as white powder.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. filtrationThe catalyst was filtered
  2. washwashed with 2-propanol
  3. concentrationthe filtrate was concentrated
  4. additionEthanol (10 ml)-hexane (50 ml) was added to the residue
  5. customto produce
  6. filtrationIt was then filtered
  7. washwashed with 10 ml of ethanol
  8. customdrying

出典と根拠

ORDレコード
ord-b94a7eedcb6a491bb16c395c0a673a75
出典データセット
uspto-grants-2009_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07531532B2

反応ノート

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