HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 3,4-Difluorophenoxymethyl vinyl ketone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-(3,4-Difluorophenoxy)acetic acid | HCID 302915 | — |
| Reactant | HCID 178418507 | HCID 178418507 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 3,4-Difluorophenoxymethyl vinyl ketone | HCID 22114232 | — |
Reaction Steps
To a suspension of 3,4-difluorophenoxy acetic acid (5.00 g, 25.7 mmol) lithium salt in DME (20 mL) was added to a 1M THF solution of vinyl magnesium bromide (38 mmol). After a period of 18 h, the resulting clear solution was poured over 1N HCl (67 mL). The aqueous phase was then extracted with Et2O. The ethereal phase was washed with H2O, 1M K2CO3 then H2O. After drying over MgSO4 and evaporation an orange oil was obtained and used as such for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06020343 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-ae75424a26ac4acab92f83af0b128957 |
| Source note | uspto-grants-2000_02 |