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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672702Generated: October 30, 2026

Ammonium Chloride → Methyl E-4-{6-cyano-2-[2-(2-hydroxyphenyl)vinyl]hexyl}benzoate

https://huagongshe.com/reaction/1672702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant(2-Hydroxybenzyl)triphenylphosphonium bromideHCID 2724142—
ReactantMethyl 4-(6-cyano-2-formylhexyl)benzoateHCID 57864395—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductMethyl E-4-{6-cyano-2-[2-(2-hydroxyphenyl)vinyl]hexyl}benzoateHCID 5786436064%

Reaction Steps

14.34 ml (35.85 mmol) of a 2.5 M solution of n-butyllithium in hexane are slowly added to a solution of 5.753 g (12.81 mmol) of (2-hydroxybenzyl)triphenylphosphonium bromide in 300 ml of anhydrous THF at 0° C. Then, at this temperature, 3.5 g (12:81 mmol) of methyl 4-(6-cyano-2-formylhexyl)benzoate from Example 118A are slowly metered in. After warming to room temperature, the reaction solution is stirred for 4 hours, then mixed with saturated ammonium chloride solution and concentrated to dryness. The residue is taken up in ethyl acetate, washed with water and saturated sodium chloride solution and dried over sodium sulfate. After filtration, the solvent is concentrated to dryness. The resulting crude product is purified by flash chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 4:1). 2976 mg (64% yield) of a colorless solid are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998988B2
Source datasetuspto-grants-2011_08
ORD IDord-12d680bebde1442dba4c9355c105b9bc
Source noteuspto-grants-2011_08