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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429615Generated: October 31, 2026

Ammonium Chloride → (S)-1-(2,3-difluorophenyl)-2-((1,1,1-trifluorobut-3-en-2-yl)oxy)ethanone

https://huagongshe.com/reaction/1429615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium BicarbonateHCID 516892—
Reactant1-Bromo-2,3-difluorobenzeneHCID 2733260—
Reactant(S)-N-Methoxy-N-methyl-2-((1,1,1-trifluorobut-3-en-2-yl)oxy)acetamideHCID 86668361—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
Product(S)-1-(2,3-difluorophenyl)-2-((1,1,1-trifluorobut-3-en-2-yl)oxy)ethanoneHCID 70497436—

Reaction Steps

A solution of n-butyllithium in hexane (2.50 M, 13.5 mL) was added dropwise over 20 mins to a solution containing 1-bromo-2,3-difluorobenzene (6.50 g) in Et2O (50 mL) under a N2 atmosphere at −78° C. The reaction solution was allowed to stir for 60 mins. (S)—N-Methoxy-N-methyl-2-((1,1,1-trifluorobut-3-en-2-yl)oxy)acetamide) (5.20 g) in Et2O (10 mL) was then added dropwise to the reaction solution, and after stirring at −78° C. for 1 h, aqueous NH4Cl (50 mL) was added to the reaction solution, followed by warming to RT. NaHCO3 (sat. aq., 100 mL) was added to the reaction solution, and the mixture was extracted with EtOAc (3×100 mL). The combined organic portions were dried over MgSO4, evaporated, and the residue was purified by silica gel column chromatography (1% to 10% EtOAc in hexanes) to obtain the title compound (3.91 g). 1H NMR (400 MHz, CDCl3) δ ppm: 4.33-4.43 (m, 1H), 4.80-4.84 (m, 2 H), 5.55-5.67 (m, 2 H), 5.76-5.94 (m, 1 H), 7.18-7.28 (m, 1 H), 7.37-7.47 (m, 1 H), 7.70 (ddt, J=7.9, 6.0, 1.7 Hz, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940734B2
Source datasetuspto-grants-2015_01
ORD IDord-5b176074275a40939bba5fa04ada7e75
Source noteuspto-grants-2015_01