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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354705Generated: October 31, 2026

1-(Bromomethyl)-3-phenoxybenzene → 3-Phenoxybenzyl alpha-fluoro-alpha-isopropylphenylacetate

https://huagongshe.com/reaction/354705

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Bromomethyl)-3-phenoxybenzeneHCID 94544—
Reactantalpha-Fluoro-3-phenoxybenzyl alpha-isopropyl-4-chlorophenylacetateHCID 20507332—
Reactantalpha-Fluoro-alpha-isopropylphenylacetic acidHCID 54262117—
Product3-Phenoxybenzyl alpha-fluoro-alpha-isopropylphenylacetateHCID 54191148—

Reaction Steps

This compound was prepared from 3-phenoxybenzyl bromide and α-fluoro-α-isopropylphenylacetic acid following the method used in Example 2 Method B for the preparation of α-fluoro-3-phenoxybenzyl α-isopropyl-4-chlorophenylacetate. The product, a colourless oil, was characterised by pmr spectroscopy. Chemical shift ppm (solvent CDCl3): 0.69(3H, d, J=6 Hz, CH3); 1.05 (3H, d of d, J=6 Hz and J=2 Hz, CH3); 2.34(1H, m, CH(CH3)2); 3.27 (1H, d, J=10 Hz, CH); 7.17(1H, d of d, J=56 Hz and J=2 Hz, CHF) and c. 7.20(14H, m, aromatic protons).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04376784
Source datasetuspto-grants-1983_03
ORD IDord-92b6fd9b7dee4459837ae2b55880cb16
Source noteuspto-grants-1983_03