HuagongsheHuagongshe Chemistry Print Report · For research reference only
Z-(1R,S)-cis-2,2-dimethyl-3-(2,2-chloro-3,3,3-trifluoro-1-propenyl)cyclopropanecarboxylic acid → alpha-Fluoro-3-phenoxybenzyl 3-(2-chloro-2-trifluoromethylvinyl)2,2-dimethylcyclopropanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Z-(1R,S)-cis-2,2-dimethyl-3-(2,2-chloro-3,3,3-trifluoro-1-propenyl)cyclopropanecarboxylic acid | HCID 156507 | — |
| Reactant | alpha-Fluoro-3-phenoxybenzylbromide | HCID 13194583 | — |
| Product | alpha-Fluoro-3-phenoxybenzyl 3-(2-chloro-2-trifluoromethylvinyl)2,2-dimethylcyclopropanecarboxylate | HCID 54451260 | — |
Reaction Steps
This compound was prepared from 3-(2-chloro-2-trifluoromethylvinyl)-2,2-dimethylcyclopropanecarboxylic acid and α-fluoro-3-phenoxybenzyl bromide following the procedure described in Example 2 Method B. The product, a colourless oil, was characterised by pmr spectroscopy. Chemical shift δppm (solvent CDCl3): 1.26 (6H, m, C(CH3)2); 1.72-2.44 (2H, m, cyclopropyl protons); 5.80 and 6.18 (1H, 2xd, vinyl proton); 7.20 (1H, d, J=56 Hz, CHF) and about 7.13 (9H, m, aromatic protons).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04376784 |
| Source dataset | uspto-grants-1983_03 |
| ORD ID | ord-562e23180318471d87e180bf04325608 |
| Source note | uspto-grants-1983_03 |