HuagongsheHuagongshe Chemistry Print Report · For research reference only
alpha-Ethynyl-4-fluoro-3-phenoxybenzyl alcohol → alpha-Ethynyl-4-fluoro-3-phenoxybenzyl 4-(4-fluorophenyl)-2-isopropyl-3-butenoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | alpha-Ethynyl-4-fluoro-3-phenoxybenzyl alcohol | HCID 14457404 | — |
| Reactant | 1-(4-Fluoro-3-phenoxyphenyl)ethanol | HCID 19754841 | — |
| Reactant | 2-Isopropyl-4-(4-fluorophenyl)-3-butenoic acid | HCID 53885514 | — |
| Product | alpha-Ethynyl-4-fluoro-3-phenoxybenzyl 4-(4-fluorophenyl)-2-isopropyl-3-butenoate | HCID 54345861 | — |
| Product | 4-Fluoro-alpha-methyl-3-phenoxybenzyl 4-(4-fluorophenyl)-2-isopropyl-3-butenoate | HCID 54357547 | — |
Reaction Steps
Each of α-ethynyl-4-fluoro-3-phenoxybenzyl alcohol and 4-fluoro-α-methyl-3-phenoxybenzyl alcohol is reacted with 4-(4-fluorophenyl)-2-isopropyl-3-butenoic acid to yield α-ethynyl-4-fluoro-3-phenoxybenzyl 4-(4-fluorophenyl)-2-isopropyl-3-butenoate and 4-fluoro-α-methyl-3-phenoxybenzyl 4-(4-fluorophenyl)-2-isopropyl-3-butenoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04229368 |
| Source dataset | uspto-grants-1980_10 |
| ORD ID | ord-13d1faefb17e44c99a514b5950c154f9 |
| Source note | uspto-grants-1980_10 |