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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 894337Generated: October 26, 2026

Water → alpha-Fluoro-3-phenoxybenzyl alpha-isopropyl-4-chlorophenylacetate

https://huagongshe.com/reaction/894337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantalpha-Fluoro-3-phenoxybenzylbromideHCID 13194583—
ReactantPotassium alpha-isopropyl-4-chlorophenylacetateHCID 23685460—
SolventDimethylformamideHCID 6228—
Productalpha-Fluoro-3-phenoxybenzyl alpha-isopropyl-4-chlorophenylacetateHCID 2050733241.4%

Reaction Steps

A mixture of potassium α-isopropyl-4-chlorophenylacetate (0.91 g) and α-fluoro-3-phenoxy benzyl bromide (1.06 g) in dimethylformamide (10 ml) was stirred at ambient temperature over a period of 2 hours. The reaction mixture was poured into water and the aqueous solution was extracted with diethyl ether. The ether extract was washed with aqueous sodium carbonate solution and was then dried over anhydrous sodium sulfate. The ether was removed by distillation under reduced pressure and the residue chromatographed over silica gel to give α-fluoro-3-phenoxybenzyl α-isopropyl-4-chlorophenylacetate (0.62 g; 37%) as a colourless oil. The product was characterised by pmr spectroscopy. Chemical shift δppm (solvent CDCl3): 0.69(3H, d, J=6Hz, CH3); 1.05(3H, d of d, J=6Hz and J=2Hz, CH3); 2.34(1H, m, --CH(CH3)2); 3.29 (1H, d, J=10Hz, CH); 7.22(1H, d of d, J=56Hz and J= 2Hz, CHF) and c. 7.24(13H, m, aromatic protons).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04283414
Source datasetuspto-grants-1981_08
ORD IDord-6fe6199aa5a045ad9efd3530f7f17c09
Source noteuspto-grants-1981_08