HuagongsheHuagongshe Chemistry Print Report · For research reference only
alpha-Cyano-2-fluoro-5-phenoxybenzyl alcohol → 3-Fluoro-5-phenoxybenzyl 2-(2-fluoro-4-trifluoromethylphenylamino)-3-methylbutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | alpha-Cyano-2-fluoro-5-phenoxybenzyl alcohol | HCID 20236070 | — |
| Reactant | 2-(2-Fluoro-4-trifluoromethylphenylamino)-3-methylbutanoic acid | HCID 20283983 | — |
| Reactant | 3-Fluoro-5-phenoxybenzyl alcohol | HCID 53813367 | — |
| Product | 3-Fluoro-5-phenoxybenzyl 2-(2-fluoro-4-trifluoromethylphenylamino)-3-methylbutanoate | HCID 53707768 | — |
| Product | alpha-Cyano-2-fluoro-5-phenoxybenzyl 2-(2-fluoro-4-trifluoromethylphenylamino)3-methylbutanoate | HCID 54005306 | — |
Reaction Steps
The alcohol, α-cyano-2-fluoro-5-phenoxybenzyl alcohol and 3-fluoro-5-phenoxybenzyl alcohol, is reacted with 2-(2-fluoro-4-trifluoromethylphenylamino)-3-methylbutanoic acid to yield α-cyano-2-fluoro-5-phenoxybenzyl 2-(2-fluoro-4-trifluoromethylphenylamino)3-methylbutanoate and 3-fluoro-5-phenoxybenzyl 2-(2-fluoro-4-trifluoromethylphenylamino)-3-methylbutanoate, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04231953 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-4dafdcfd533f4d36962db01448e78805 |
| Source note | uspto-grants-1980_11 |