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Barium hydroxide, octahydrate → 4-Amino-1-methylpiperidine-4-carboxylic acid

HRID 1458766
ノート
印刷プレビュー

反応式

HRID 1458766 の反応式
CN1CCC2(NC(=O)NC2=O)CC1.[NH2:14][C:15]1([C:22]([OH:24])=[O:23])[CH2:20][CH2:19][N:18]([CH3:21])[CH2:17][CH2:16]1.O.O.O.O.O.O.O.O.[OH-].[Ba+2].[OH-]>O>[NH2:14][C:15]1([C:22]([OH:24])=[O:23])[CH2:16][CH2:17][N:18]([CH3:21])[CH2:19][CH2:20]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 17749109Barium hydroxide, octahydrateHCID 67633729HCID 67633729、化合物

生成物 1

HCID 2729544-Amino-1-methylpiperidine-4-carboxylic acid収率 379.5%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

4-Amino-1-methylpiperidine-4-carboxylic acid 1-methylpiperidine-4-spiro-5'-hydantoin (9.75 g., 0.0533 mole) and barium hydroxide octahydrate (28.8 g., 0.00913 mole) in water (150 ml.) were heated at 160° C. in an autoclave for three hours. The contents of four such batches were combined and the precipitated barium carbonate was filtered off. The filtrate was neutralized with solid carbon dioxide and the precipitate was removed by filtration. The filtrate was concentrated to a small volume to give 4-amino1-methylpiperidine-4-carboxylic acid (32.0 g., 95% yield), m.p. 275°-280° C. (dec.).

後処理

  1. filtrationthe precipitated barium carbonate was filtered off
  2. customthe precipitate was removed by filtration
  3. concentrationThe filtrate was concentrated to a small volume

出典と根拠

ORDレコード
ord-d054453e618c4a609217e9c09f5a19e1
出典データセット
uspto-grants-1998_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05852029

反応ノート

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