HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-Methoxyphenyl)-3-methylbutanoic acid → alpha-Fluoro-3-phenoxybenzyl alpha-isopropyl-(4-methoxyphenyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-Methoxyphenyl)-3-methylbutanoic acid | HCID 182674 | — |
| Reactant | alpha-Fluoro-3-phenoxybenzylbromide | HCID 13194583 | — |
| Product | alpha-Fluoro-3-phenoxybenzyl alpha-isopropyl-(4-methoxyphenyl)acetate | HCID 53940984 | — |
Reaction Steps
This compound was prepared from α-isopropyl-(4-methoxyphenyl)acetic acid and α-fluoro-3-phenoxybenzylbromide following the procedure described in Example 2 Method B. The product, a colourless oil, was characterised by pmr spectroscopy. Chemical shift δppm (solvent CDCl3): 0.72 (3H, d, J=6 Hz, CH3); 1.06 (3H, d of d, J=6 Hz and J=2 Hz, CH3); about 2.25 (1H, m, --CH(CH3)2); 3.17 (1H, d, J=10 Hz, CH); 3.76 (3H, s, CH3O); 7.18 (1H, d of d, J=56 Hz and J=2 Hz, CHF); about 7.2 (13H, m, aromatic protons).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04376784 |
| Source dataset | uspto-grants-1983_03 |
| ORD ID | ord-135e99a3dba74dae8986303181da10f0 |
| Source note | uspto-grants-1983_03 |