HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 58333155, compound → HCID 58964468, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 58333155 | HCID 58333155 | — |
| Catalyst | HCID 178425456 | HCID 178425456 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58964468 | HCID 58964468 | — |
Reaction Steps
To a solution of 2-allyloxy-2-trifluoromethyl-but-3-enoic acid ethyl ester (2.15 g, see above) in CH2Cl2 (100 mL) at room temperature was added Grubbs catalyst 2nd generation (Aldrich) (67 mg). The resulting mixture was stirred for 18 h at room temperature. The reaction mixture was then filtered through a plug of Celite® and silica gel, rinsed with EtOAc and then concentrated to yield the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09120830B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-803471e1148b43738307ed2a424b8194 |
| Source note | uspto-grants-2015_09 |