HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Z-4-(2,3-dichloroprop-2-en-1-yl)-2,3,5,6-tetrafluorobenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 2,3,5,6-Tetrafluoro-4-(2-propyn-1-yl)benzyl Alcohol | HCID 11435909 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Z-4-(2,3-dichloroprop-2-en-1-yl)-2,3,5,6-tetrafluorobenzyl alcohol | HCID 13911484 | — |
Reaction Steps
A solution of 4-(prop-2-yn-1-yl)-2,3,5,6-tetrafluorobenzyl alcohol (0.1 g) copper (II) chloride (1.3 g), and lithium chloride (0.62 g) in dry acetonitrile (23 cm3) was heated at the reflux temperature for 40 hours. The resulting dark solution was poured into dilute hydrochloric acid, and extracted into ethyl acetate. The organic phase was washed with more dilute hydrochloride acid, dried, and the solvent evaporated under reduced pressure to give Z-4-(2,3-dichloroprop-2-en-1-yl)-2,3,5,6-tetrafluorobenzyl alcohol (0.1 g) as an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04762835 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-cc6c5d1acedf4d1b8e540664a279825e |
| Source note | uspto-grants-1988_08 |