1,2-Hydrazinedicarboxamide → 4-Stearyl-1,2,4-triazolidine-3,5-dione

HRID 355029

反応式

HRID 355029 の反応式
[C:1]([NH:4][NH:5][C:6]([NH2:8])=[O:7])(N)=[O:2].[CH2:9](N)[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]>CN1CCCC1=O>[CH2:26]([N:8]1[C:6](=[O:7])[NH:5][NH:4][C:1]1=[O:2])[CH2:25][CH2:24][CH2:23][CH2:22][CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH3:9]

参加物

4

反応物 2

HCID 80391,2-HydrazinedicarboxamideHCID 15793Octadecylamine

生成物 1

HCID 204728254-Stearyl-1,2,4-triazolidine-3,5-dione

試薬・触媒・溶媒 1

HCID 13387N-methyl-2-pyrrolidone溶媒

実験手順

360 g of hydrazodicarbonamide, 807 g of stearyl amine and 1 ml of tin(II)dioctoate are stirred in 1 liter of N-methyl pyrrolidone for 4 hours at 175° C. and for 6 hours at 200° C. A deposit precipitates on cooling and is isolated by filtration under suction and washed with water, giving 955 g (90% of the theoretical) of 4-stearyl-1,2,4-triazolidine-3,5-dione in the form of colourless crystals melting at 118° to 120° C.

後処理

  1. customA deposit precipitates
  2. temperatureon cooling
  3. customis isolated by filtration under suction
  4. washwashed with water

出典と根拠

ORDレコード
ord-a571555c2a1c434a8ef606d601ab447a
出典データセット
uspto-grants-1983_03
特許番号
US04377694

関連ノート

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