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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646395Generated: October 30, 2026

Ammonium Chloride → HCID 67002199, compound

https://huagongshe.com/reaction/646395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Bromo-3-formylbenzonitrileHCID 22574902—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 57744084HCID 57744084—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 67002199HCID 6700219944.5%

Reaction Conditions

Temperature-25 °C

Reaction Steps

Diethyl (4-trifluoromethoxybenzyl)phosphonate (7.8 g) was dissolved in 100 mL of DMF, 5.0 g of 4-bromo-3-formyl-benzonitrile was added, and the mixture was cooled to −25° C. Potassium tert-butoxide (6.4 g) was added, and the mixture was stirred for 2 hours at −25° C. To the reaction mixture, 100 mL of a saturated aqueous solution of ammonium chloride and 100 mL of water were added, and the mixture was extracted 3 times with ethyl acetate (100 mL). The respective organic layers were combined, whereafter the combined organic layer was washed with water and a saturated aqueous solution of sodium chloride, and dried over magnesium sulfate. The magnesium sulfate was separated by filtration, and the filtrate was concentrated under reduced pressure. The residue was subjected to 100 g silica gel column chromatography to obtain 3.9 g of 4-bromo-3-[2-(4-trifluoromethoxy-phenyl)-vinyl]-benzonitrile as a crude product with the use of an eluant (ethyl acetate and n-hexane, 1:10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07705053B2
Source datasetuspto-grants-2010_04
ORD IDord-bf7e9a46450142ddb04d230a7079129b
Source noteuspto-grants-2010_04