HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733271Generated: October 25, 2026
Phthalaldehydic acid → 2-(2-Ethoxycarbonylpropen-1-yl)benzoic acid
https://huagongshe.com/reaction/733271
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phthalaldehydic acid | HCID 8406 | — |
| Reactant | Ethyl 2-(triphenylphosphoranylidene)propionate | HCID 79792 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-Ethoxycarbonylpropen-1-yl)benzoic acid | HCID 69054538 | — |
Reaction Steps
A mixture of 5.0 g (33.3 mmol) of 2-formylbenzoic acid and 14.5 g (40.0 mmol) of ethyl 2-(triphenylphosphanylidene)propionate in 100 cm3 of dimethylformamide is stirred at a temperature in the region of 20° C. for 1 hour. After removal of the solvent, the residue is dissolved in dichloromethane and then extracted twice with sodium bicarbonate solution. The aqueous phases are combined, washed with dichloromethane and then acidified with aqueous 6N hydrochloric acid solution to a pH of between 1 and 2. After extracting twice with dichloromethane, the organic phases are combined, dried over magnesium sulfate and then concentrated. 2-(2-Ethoxycarbonylpropen-1-yl)benzoic acid is thus obtained in the form of a yellow oil, which is used directly in the following step without further purification
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07589117B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-545d938c4a0440d393ce25374513dc26 |
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| Source note | uspto-grants-2009_09 |
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