tert-Butyl isocyanate → HCID 20543608、化合物
反応式
[CH3:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[C:3]=1[NH:9][C:10]([NH2:12])=[S:11].[C:13]([N:17]=[C:18]=[O:19])([CH3:16])([CH3:15])[CH3:14]>C1(C)C(C)=CC=CC=1>[CH3:8][C:4]1[CH:5]=[CH:6][CH:7]=[C:2]([CH3:1])[C:3]=1[NH:9][C:10]([NH:12][C:18](=[O:19])[NH:17][C:13]([CH3:16])([CH3:15])[CH3:14])=[S:11]参加物
4
実験手順
To a mixture of 8.8 g. (0.05 mole) of 1-(2,6-dimethylphenyl)thiourea and 10 ml. of xylene is added 5 g. of t-butylisocyanate (0.05 mole) and the mixture is refluxed for 2 hours. The reaction product is cooled, triturated with heptane and filtered. Recrystallization from 1:1 isopropanol/water results in 1-(2,6-dimethylphenyl)-3-(t-butylcarbamyl)thiourea.
後処理
- additionTo a mixture of 8.8 g
- temperatureThe reaction product is cooled
- customtriturated with heptane
- filtrationfiltered
- customRecrystallization from 1:1 isopropanol/water
- customresults in 1-(2,6-dimethylphenyl)-3-(t-butylcarbamyl)thiourea
出典と根拠
- ORDレコード
- ord-84928cef24dc45059285e946fac1761e
- 出典データセット
- uspto-grants-1977_05
- 特許番号
- US04025652
反応ノート
読み込み中…