HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dichloropropene → HCID 14819356, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dichloropropene | HCID 6565 | — |
| Reactant | 4-Fluorophenol | HCID 9732 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 14819356 | HCID 14819356 | 79% |
Reaction Steps
According to the procedure of W. K. Anderson et al., J. Chem. Soc., Perkin 1,1 (1976), a mixture of 4-fluorophenol (20.0 g, 0.178 mol) and K2CO3 (27.3 g, 0.196 mol) in acetone (250 mL) was heated at reflux for 1 hour. 2,3-Dichloro-1-propene was added, and the resulting mixture was refluxed for 2 days, cooled, and concentrated. The mixture was diluted with H2O, and extracted with ether (3×150 mL). The ethereal extracts were dried (MgSO4) and concentrated to give a brown oil. Distillation under high vacuum gave 26.4 g (79%) of product as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04895860 |
| Source dataset | uspto-grants-1990_01 |
| ORD ID | ord-0889d291dbb4401680730b9cf407a9a0 |
| Source note | uspto-grants-1990_01 |