HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Fluoro-3-phenoxyphenyl)methanol → 4-Fluoro-3-phenoxybenzyl 3-(i-butoxy)-2,2-dimethylcyclopropanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Fluoro-3-phenoxyphenyl)methanol | HCID 12874224 | — |
| Reactant | (2-Fluoro-5-phenoxyphenyl)methanol | HCID 15681057 | — |
| Reactant | 3-(i-Butoxy)-2,2-dimethylcyclopropanecarboxylic acid | HCID 54542542 | — |
| Product | 4-Fluoro-3-phenoxybenzyl 3-(i-butoxy)-2,2-dimethylcyclopropanecarboxylate | HCID 23338880 | — |
| Product | 2-Fluoro-5-phenoxybenzyl 3-(i-butoxy)-2,2-dimethylcyclopropanecarboxylate | HCID 54242770 | — |
Reaction Steps
Using the procedure of Example 14, each of 4-fluoro-3-phenoxybenzyl alcohol and 2-fluoro-5-phenoxybenzyl alcohol is reacted with 3-(i-butoxy)-2,2-dimethylcyclopropanecarboxylic acid to yield 4-fluoro-3-phenoxybenzyl 3-(i-butoxy)-2,2-dimethylcyclopropanecarboxylate and 2-fluoro-5-phenoxybenzyl 3-(i-butoxy)-2,2-dimethylcyclopropanecarboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04225533 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-3728e506000b471c9235231062fcac3b |
| Source note | uspto-grants-1980_09 |