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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (2-Hydroxybenzyl)triphenylphosphonium bromide | HCID 2724142 | — |
| Reactant | Methyl 4-(6-cyano-2-formylhexyl)benzoate | HCID 57864395 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Methyl E-4-{6-cyano-2-[2-(2-hydroxyphenyl)vinyl]hexyl}benzoate | HCID 57864360 | 64% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07998988B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-12d680bebde1442dba4c9355c105b9bc |
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| Source note | uspto-grants-2011_08 |
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