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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894346Generated: October 30, 2026

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

https://huagongshe.com/reaction/894346

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 δ ppm (solvent CDCl3): 0.72(3H, d, J=6Hz, CH3); 1.06(3H, d of d, J=6Hz and J=2Hz, CH3); about 2.25(1H, m, --CH(CH3)2); 3.17(1H, d, J=10Hz, CH); 3.76(3H, s, CH3O); 7.18(1H, d of d, J=56Hz and J=2Hz, CHF); about 7.2(13H, m, aromatic protons).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04283414
Source datasetuspto-grants-1981_08
ORD IDord-e2c3956170064374ae5cef7e0e2e2f1a
Source noteuspto-grants-1981_08