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Sodium Carbonate → N,N'-bis(chloroacetyl)-trans-1,2-diaminocyclohexane

HRID 1708331
ノート
印刷プレビュー

反応式

HRID 1708331 の反応式
C(=O)([O-])[O-].[Na+].[Na+].[Cl:7][CH2:8][C:9]([NH:11][C@@H:12]1[CH2:17][CH2:16][CH2:15][CH2:14][C@H:13]1[NH:18][C:19](=[O:22])[CH2:20][Cl:21])=[O:10].[NH2:23][C@@H:24]1[CH2:29][CH2:28][CH2:27][CH2:26][C@H:25]1[NH2:30]>C(#N)C>[Cl:7][CH2:8][C:9]([NH:11][C@@H:12]1[CH2:17][CH2:16][CH2:15][CH2:14][C@H:13]1[NH:18][C:19](=[O:22])[CH2:20][Cl:21])=[O:10].[O:22]=[C:19]1[CH2:20][NH:30][CH:25]2[CH:24]([CH2:29][CH2:28][CH2:27][CH2:26]2)[NH:23][CH2:8][C:9](=[O:10])[NH:11][CH:12]2[CH:13]([CH2:14][CH2:15][CH2:16][CH2:17]2)[NH:18]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 10340Sodium Carbonate2 回HCID 438061,2-Diaminocyclohexane, trans-HCID 10061487N,N'-bis(chloroacetyl)-trans-1,2-diaminocyclohexane

生成物 2

HCID 10061487N,N'-bis(chloroacetyl)-trans-1,2-diaminocyclohexaneHCID 53848153HCID 53848153、化合物

試薬・触媒・溶媒 1

HCID 6342
Acetonitrile
溶媒

反応条件

温度
82 °C

実験手順

N,N'-bis(chloroacetyl)-trans-1,2-diaminocyclohexane was prepared according to the procedure outlined by Saburi, M. and Yoshikawa, S., "Stereochemical studies of N-methyl-(S)-alaninatocobalt(III) complexes with chiral tetraamines. II. Cobalt(III)-N-methyl(S)- and (R)-alaninate-N,N'-bis(β-aminoethyl)-1(R), 2(R)-diaminocyclohexane systems," Bull. Chem. Soc. Jpn., 1974, 47, 1184-1189. Anhydrous sodium carbonate (250 g., 2.36 mol.) was added to a solution of 33.4 g. (125 mmol.) of N,N'-bis(chloroacetyl)-trans-1,2-diaminocyclohexane and 15 ml. (125 mmol.) of trans-1,2diaminocyclohexane in 3750 ml. of acetonitrile. The temperature was raised to 82° C., and the reaction mixture was violently agitated for 20 hours. At the end of the reaction, sodium carbonate was eliminated by filtration and the solvent was evaporated under vacuum. The solid residue was recrystallized from ethanol. Up to five successive batches of the desired compound were obtained after the progressive concentration of the ethanolic solution under vacuum. The yield was 9.6 g. of compound (A) as a white powder.

後処理

  1. filtrationwas eliminated by filtration
  2. customthe solvent was evaporated under vacuum
  3. customThe solid residue was recrystallized from ethanol

出典と根拠

ORDレコード
ord-2f8f515068764af3bee71f7fa6981350
出典データセット
uspto-grants-1994_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05358704

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート