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Carbon Disulfide → HCID 12694981、化合物

HRID 67967
ノート
印刷プレビュー

反応式

HRID 67967 の反応式
[NH2:1][C@@H:2]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([Br:12])[CH:10]=2)[CH2:5][CH2:4][C@H:3]1[NH2:13].[C:14](=S)=[S:15]>C(O)C>[Br:12][C:9]1[CH:10]=[C:11]2[C:6]([CH2:5][CH2:4][C@H:3]3[NH:13][C:14](=[S:15])[NH:1][C@@H:2]32)=[CH:7][CH:8]=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 6348Carbon DisulfideHCID 12694952Trans-1,2-diamino-7-bromo-1,2,3,4-tetrahydronaphthalene

生成物 1

HCID 12694981HCID 12694981、化合物収率 70%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

Trans-1,2-diamino-7-bromo-1,2,3,4-tetrahydronaphthalene (6.75 g, 28.0 m mol) was dissolved in ethanol (70 ml) and carbon disulfide (1.9 ml, 31.7 m mol) was added to the solution. After stirring at room temperature for 20 minutes, they were heated under reflux for 5.5 hours. The reaction mixture was cooled in an ice bath and crystals precipitated were collected by filtration, whereby trans-8-bromo-3a,4,5,9b-tetrahydronaphth[1,2-d]imidazoline-2-thione (5.57 g) was obtained in 70% yield. The crystals were recrystallized from methanol-acetonitrile to give pale-yellow crystals melting at 259.5°-260.5° C. (decomposition). The product gave the following data on spectroscopy and elemental analysis.

後処理

  1. temperaturethey were heated
  2. temperatureunder reflux for 5.5 hours
  3. temperatureThe reaction mixture was cooled in an ice bath
  4. customcrystals precipitated
  5. filtrationwere collected by filtration

出典と根拠

ORDレコード
ord-f0c86e4bd77944dfb5b53e3dff19e272
出典データセット
uspto-grants-1982_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04347369

反応ノート

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