HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927283Generated: November 1, 2026
Benzenepropanoic acid → HCID 12740364, compound
https://huagongshe.com/reaction/1927283
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenepropanoic acid | HCID 107 | — |
| Reactant | Cyanoacetic acid | HCID 9740 | — |
| Reactant | Benzenepropanoyl chloride | HCID 64801 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 12740364 | HCID 12740364 | — |
Reaction Steps
A solution of cyanoacetic acid (1.0 g, 11.8 mmol) in tetrahydrofuran (20 mL) was cooled to −78° C. and treated with 1.6 M n-butyl lithium in hexanes (14.7 mL, 23.5 mmol). The mixture was warmed to −20° C. over 2 hours, cooled to −78° C. and treated with 3-phenylpropionyl chloride (prepared by refluxing a solution of 3-phenylpropionic acid (1.0 g, 6.7 mmol) in thionyl chloride (4 mL) for 3 hours, evaporating and drying). The mixture was stirred at −78° C. for 1 hour and 20% hydrochloric acid added until the pH=3. The mixture was diluted with diethyl ether, washed with saturated sodium bicarbonate, and the organic layer separated and concentrated. The crude product was purified by flash chromatography on silica gel using 0-50% ethyl acetate/hexanes to provide the title compound. MS (ESI) m/e 191 (M+H+NH3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183250B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-76a61b00b8424ba59897327eaa48cb5f |
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| Source note | uspto-grants-2012_05 |
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