HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913763Generated: October 25, 2026
Potassium Carbonate → Methyl 4-[(3E)-2-[2-(4-cyanophenyl)ethyl]-4-(2-{[4-(2-phenylethyl)benzyl]oxy}phenyl)but-3-en-1-yl]benzoate
https://huagongshe.com/reaction/1913763
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Phenethylbenzyl chloride | HCID 2733990 | — |
| Reactant | HCID 57831366 | HCID 57831366 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 4-[(3E)-2-[2-(4-cyanophenyl)ethyl]-4-(2-{[4-(2-phenylethyl)benzyl]oxy}phenyl)but-3-en-1-yl]benzoate | HCID 59180519 | 70% |
Reaction Steps
460 mg (2 mmol) of 1-(chloromethyl)-4-(2-phenylethyl)benzene [preparation according to M. Carrara et al., Arzneim. Forsch. 47 (7), 803-809 (1997)] and 414 mg (3 mmol) of anhydrous potassium carbonate are added to a solution of 411 mg (1 mmol) of methyl 4-[(3E)-2-[2-(4-cyanophenyl)ethyl]-4-(2-hydroxyphenyl)but-3-en-1-yl]benzoate in 10 ml of dry acetonitrile, and the mixture is heated under reflux for 12 hours. The mixture is then evaporated to dryness. The residue is taken up in ethyl acetate, washed with water and with saturated sodium chloride solution and dried over sodium sulphate. After filtration, the organic phase is evaporated and the resulting crude product is purified by preparative HPLC. 431 mg (0.7 mmol, 65% yield) of a solid are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08609727B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-6e3b0143a7e64b6aa9a59d81e3c223a8 |
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| Source note | uspto-grants-2013_12 |
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