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Potassium Carbonate → 2-Methylimino-3-methyl-5-benzyl-tetrahydro-1,3,5-thiadiazin-4-one

HRID 237074
ノート
印刷プレビュー

反応式

HRID 237074 の反応式
[CH2:1]([N:8]([CH2:12]Cl)[C:9](Cl)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:14][NH:15][C:16]([NH:18][CH3:19])=[S:17].C(=O)([O-])[O-].[K+].[K+]>C(O)C>[CH3:14][N:15]=[C:16]1[N:18]([CH3:19])[C:9](=[O:10])[N:8]([CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[CH2:12][S:17]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 3

HCID 11430Potassium CarbonateHCID 2723631N,N'-DimethylthioureaHCID 21314706N-benzyl-N-chloromethylcarbamoyl chloride

生成物 1

HCID 213147022-Methylimino-3-methyl-5-benzyl-tetrahydro-1,3,5-thiadiazin-4-one収率 80.2%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

A mixture of 4.4 g (0.02 mole) of N-benzyl-N-chloromethylcarbamoyl chloride and 2.0 g (0.02 mole) of 1,3-dimethylthiourea was dissolved in 50 ml of ethyl alcohol and heated under reflux with stirring for 2 hours. After addition of 20 ml of a saturated aqueous potassium carbonate solution, the mixture was extracted with 100 ml of benzene. The benzene layer was washed with water, dried, and freed from the benzene by distillation under reduced pressure to obtain 4.0 g of crude crystals which were recrystallized from ether. Yield 3.2 g (63%); m.p. 93°-95° C.

後処理

  1. temperatureheated
  2. temperatureunder reflux
  3. extractionthe mixture was extracted with 100 ml of benzene
  4. washThe benzene layer was washed with water
  5. customdried
  6. distillationfreed from the benzene by distillation under reduced pressure

出典と根拠

ORDレコード
ord-7ce92d3519144c1d8a85ec3ce9a8d49e
出典データセット
uspto-grants-1979_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04159328

反応ノート

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