Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Carbon Disulfide → 2-((Butylsulfanyl)carbonothioyl)sulfanyl)propanoic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Carbon Disulfide | HCID 6348 | — |
| 반응물 | 1-Dodecanethiol | HCID 8195 | — |
| 반응물 | 2-Bromopropionic acid | HCID 11729 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 촉매 | Tetrapropylammonium bromide | HCID 74745 | — |
| 용매 | Acetone | HCID 180 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 2-((Butylsulfanyl)carbonothioyl)sulfanyl)propanoic acid | HCID 59347154 | 111.7% |
반응 단계
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%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07745553B2 |
| 출처 데이터셋 | uspto-grants-2010_06 |
| ORD ID | ord-cbdd9b4994364bda8b1573b9e3f599bd |
| 출처 메모 | uspto-grants-2010_06 |