HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-(2-Chloroprop-2-en-1-yl)-2,3,5,6-tetrafluorobenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 13911479 | HCID 13911479 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(2-Chloroprop-2-en-1-yl)-2,3,5,6-tetrafluorobenzyl alcohol | HCID 13911480 | 99.8% |
Reaction Steps
The tetrahydropyranyl ether prepared in stage (i) (0.2 g), was dissolved in methanol (6 cm3), and to the stirred solution was added concentrated hydrochloric acid (several drops). After stirring for 6 hours, and standing for a further 14 hours, the reaction mixture was poured into water, and extracted into ethyl acetate. The organic layer was washed with water and brine, dried, and the solvent evaporated under reduced pressure to give 4-(2-chloroprop-2-en-1-yl)-2,3,5,6-tetrafluorobenzyl alcohol as an orange oil (0.15 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05132469 |
| Source dataset | uspto-grants-1992_07 |
| ORD ID | ord-9fe750ce504146e3841a9c63be6d7a98 |
| Source note | uspto-grants-1992_07 |