HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 19856768, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Thiopheneacetic acid | HCID 15970 | — |
| Reactant | 4-Bromobutyronitrile | HCID 21412 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19856768 | HCID 19856768 | — |
Reaction Steps
Thiolacetic acid (49 mL, 0.69 mol) is added to potassium carbonate (93.4 g, 0.68 mol) dissolved in water (150 mL). Ethanol (260 mL) is added and then 4-bromobutyronitrile is added at 15° to 28° C. and the reaction mixture stirred at room temperature for 16 hours. The resulting inorganic solids are filtered off and the filtrate extracted with toluene. The organic layer is separated, dried over anhydrous Na2SO4 and concentrated to give the desired 4-mercaptoacetyl butyronitrile as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04752323 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-74798945f5494e9489bbcd5db5f8baab |
| Source note | uspto-grants-1988_06 |