反応式
[Cl:1][CH2:2][CH2:3][C:4]#[N:5].[NH2:6][C:7]([NH2:9])=[S:8]>O>[ClH:1].[C:4]([CH2:3][CH2:2][S:8][C:7](=[NH:6])[NH2:9])#[N:5]参加物
4
実験手順
The 3-chloropropanenitrile (4.32 g, 48.3 mmol) and thiourea (4.04 g, 53.1 mmol) are mixed in 40 ml of water. The mixture is heated to reflux for 3 to 4 hours. The reaction mixture is evaporated and 20 ml of ethanol is added and then evaporated as well. This is repeated three times. After that, 10 ml of methanol and 30 ml of acetone are added and the mixture is stirred for one hour. The crystalline material is filtered and the product is dried under high vacuum overnight to obtain S-(2-cyanoethyl)isothiourea hydrochloride.
後処理
- temperatureThe mixture is heated
- temperatureto reflux for 3 to 4 hours
- customThe reaction mixture is evaporated
- addition20 ml of ethanol is added
- customevaporated as well
- additionAfter that, 10 ml of methanol and 30 ml of acetone are added
- filtrationThe crystalline material is filtered
- customthe product is dried under high vacuum overnight
出典と根拠
- ORDレコード
- ord-4a7cfdfb0fbb4f9ab71dc4809d8d9146
- 出典データセット
- uspto-grants-2016_05
- 特許番号
- US09340491B2
関連ノート
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