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Methyl chloroformate → Thiophamine

HRID 1415621
ノート
印刷プレビュー

反応式

HRID 1415621 の反応式
Cl[C:2]([O:4][CH3:5])=[O:3].[S-:6][C:7]#[N:8].[K+].[C:10]1([NH2:17])[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[NH2:16]>C(#N)C>[CH3:5][O:4][C:2]([NH:8][C:7]([NH:16][C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=1[NH2:17])=[S:6])=[O:3]
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 3

HCID 6586Methyl chloroformateHCID 7243O-PhenylenediamineHCID 516872Potassium thiocyanate

生成物 1

HCID 3032830Thiophamine収率 27.2%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒2 回

実験手順

Methyl chloroformate (23.6 g; 0.25 mole) was added dropwise to a stirred suspension of potassium thiocyanate (24.2 g; 0.25 mole) in dry acetonitrile (100 ml). The temperature of the reaction mixture rose spontaneously to 50° C. and stirring was continued for two hours at 45° C. to 50° C. The reaction mixture was then filtered and the clear filtrate was added dropwise during fifteen minutes to a suspension of o-phenylenediamine (27 g; 0.25 mole) in dry acetonitrile (20 ml), the temperature during the addition being maintained between 15° C. and 20° C. by external cooling. When the addition was complete, the reaction mixture was stirred at laboratory temperature for two hours, filtered, and the crude solid product was crystallised from ethanol to give colourless needles of 1-methoxycarbonyl-3-(2-aminophenyl)-thiourea (15.3 g), m.p. 183.5°-184.5° C. (with decomposition).

後処理

  1. customrose spontaneously to 50° C.
  2. filtrationThe reaction mixture was then filtered
  3. additionthe temperature during the addition
  4. temperaturebeing maintained between 15° C. and 20° C. by external cooling
  5. additionWhen the addition
  6. stirringthe reaction mixture was stirred at laboratory temperature for two hours
  7. filtrationfiltered
  8. customthe crude solid product was crystallised from ethanol

出典と根拠

ORDレコード
ord-76fe164f457f4aa9ab6b28b16e2c3693
出典データセット
uspto-grants-1977_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04005217

反応ノート

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