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Water → trans-3a,4,5,9b-Tetrahydronaphth[1,2-d]imidazoline-2-thione

HRID 67965
ノート
印刷プレビュー

反応式

HRID 67965 の反応式
[NH2:1][C@@H:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH2:5][CH2:4][C@H:3]1[NH2:12].O.[C:14](=S)=[S:15]>C(O)C>[NH:1]1[C@@H:2]2[C:11]3[C:6]([CH2:5][CH2:4][C@H:3]2[NH:12][C:14]1=[S:15])=[CH:7][CH:8]=[CH:9][CH:10]=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 962WaterHCID 6348Carbon DisulfideHCID 12694946Trans-1,2-diamino-1,2,3,4-tetrahydronaphthalene

生成物 1

HCID 12694975trans-3a,4,5,9b-Tetrahydronaphth[1,2-d]imidazoline-2-thione収率 60%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

Trans-1,2-diamino-1,2,3,4-tetrahydronaphthalene (461 mg, 2.84 m mol) was dissolved in ethanol (8 ml), water (4 ml) was added to the solution, then carbon disulfide (190 μl, 3.17 m mol) was added thereto under stirring at room temperature. The mixture was heated under reflux for 4 hours and cooled in an ice-water bath. The crystals precipitating out were separated by filtration, washed with ether and dried in vacuum to give trans-3a,4,5,9b-tetrahydronaphth[1,2-d]imidazoline-2-thione (350 mg, 1.71 m mol) in 60% yield. The data spectroscopy and elemental analysis were as follows:

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 4 hours
  3. temperaturecooled in an ice-water bath
  4. customThe crystals precipitating out
  5. customwere separated by filtration
  6. washwashed with ether
  7. customdried in vacuum

出典と根拠

ORDレコード
ord-cf447936f9cf46a789663253ae495e00
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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