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 1 M THF solution of vinyl magnesium bromide (38 mmol). After a period of 18 h, the resulting clear solution was poured over 1 N HCl (67 mL). The aqueous phase was then extracted with Et2O. The ethereal phase was washed with H2O, 1 M 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 | US06169188A |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-a9000d6790eb40e8acc65d762b4a908f |
| Source note | uspto-grants-2001_01 |