HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3,4,4-Trifluoro-3-butenoic acid, 4-nitrophenyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Nitrophenol | HCID 980 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3,4,4-Trifluoro-3-butenoyl chloride | HCID 10920789 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3,4,4-Trifluoro-3-butenoic acid, 4-nitrophenyl ester | HCID 15239190 | 92.1% |
Reaction Steps
A solution of 4-nitrophenol (1.10 g, 0.0079 mole) and 3,4,4-trifluoro-3-butenoyl chloride (1.85 g, 0.0116 mole) in dry ether (15 mL) is treated dropwise with triethylamine (1.01 g, 0.01 mole) at -78° C. with stirring. The mixture is stirred at -78° C. for 10 min and allowed to reach room temperature. The reaction mixture is diluted with ether (20 mL), stirred with 15 mL of 2N HCl. The organic layer is successively washed with water, 5% sodium bicarbonate, brine, and dried. The dark brown residue obtained after evaporation of the solvent was purified by passing through a short column of silica gel to give 1.9 g of the product as a brown solid, a 91% yield. m.p. 58°-62° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05561162 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-be89f15650534a939837522e2373f8ec |
| Source note | uspto-grants-1996_10 |