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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091013Generated: October 29, 2026

Ammonium Chloride → HCID 61262331, compound

https://huagongshe.com/reaction/2091013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant6-Methoxy-2-benzofurancarbonitrileHCID 13031369—
ReactantHCID 178420632HCID 178420632—
SolventTetrahydrofuranHCID 8028—
ProductHCID 61262331HCID 6126233139%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution (20 mL) of 6-methoxy-1-benzofuran-2-carbonitrile (1.00 g) synthesized above in tetrahydrofuran was added 1.0M cyclohexylmagnesium bromide tetrahydrofuran solution (11.5 mL), and the mixture was stirred at 50° C. overnight, and stirred with heating under reflux for 1 hr. Saturated aqueous ammonium chloride solution was added to quench the reaction, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:9, volume ratio) to give the title object compound (584 mg, 39%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-20e55043b3c44204b8afa7b45825271f
Source noteuspto-grants-2013_05