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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354709Generated: October 26, 2026

2-(4-Methoxyphenyl)-3-methylbutanoic acid → alpha-Fluoro-3-phenoxybenzyl alpha-isopropyl-(4-methoxyphenyl)acetate

https://huagongshe.com/reaction/354709

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Methoxyphenyl)-3-methylbutanoic acidHCID 182674—
Reactantalpha-Fluoro-3-phenoxybenzylbromideHCID 13194583—
Productalpha-Fluoro-3-phenoxybenzyl alpha-isopropyl-(4-methoxyphenyl)acetateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04376784
Source datasetuspto-grants-1983_03
ORD IDord-135e99a3dba74dae8986303181da10f0
Source noteuspto-grants-1983_03