化工社化工社 化学情報印刷レポート · 研究参考用
Carbon Disulfide → 2-((Butylsulfanyl)carbonothioyl)sulfanyl)propanoic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Carbon Disulfide | HCID 6348 | — |
| 反応物 | 1-Dodecanethiol | HCID 8195 | — |
| 反応物 | 2-Bromopropionic acid | HCID 11729 | — |
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 触媒 | Tetrapropylammonium bromide | HCID 74745 | — |
| 溶媒 | Acetone | HCID 180 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2-((Butylsulfanyl)carbonothioyl)sulfanyl)propanoic acid | HCID 59347154 | 111.7% |
反応手順
Dodecanethiol (2.50 g, 12.5 mmol), acetone (40 mL), and tetrapropylammonium bromide (0.27 g, 0.10 mmol) were added to a solution of sodium hydroxide (0.50 g, 12.5 mmol) in water (5 mL). The resulting solution was cooled in an ice bath and treated with carbon disulfide (0.75 mL, 0.95 g, 12.5 mmol). After 20 min, 2-bromopropanoic acid (1.91 g, 12.5 mmol) was added and the mixture was stirred at ambient temperature for 12 h. The solution was evaporated to ¼ volume and slowly acidified with 2 M hydrochloric acid (50 mL), then further diluted with water (150 mL). The resulting solid was collected and recrystallised from ether/light petroleum to give the title compound (15, R3=C12H25) as yellow crystals (3.33 g, 76%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07745553B2 |
| 出典データセット | uspto-grants-2010_06 |
| ORD ID | ord-cbdd9b4994364bda8b1573b9e3f599bd |
| 出典メモ | uspto-grants-2010_06 |