HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1722826Generated: November 2, 2026
Triphenylphosphine → 2-(2-Chlorophenyl)ethenylbenzoic acid
https://huagongshe.com/reaction/1722826
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Chlorobenzyl chloride | HCID 11906 | — |
| Reactant | 3-Hydroxyisobenzofuran-1(3H)-one | HCID 3804259 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(2-Chlorophenyl)ethenylbenzoic acid | HCID 54264772 | — |
Reaction Steps
To 78 g (297 mmol) of triphenylphosphine in 150 ml of methanol were added dropwise with stirring 48.3 g (300 mmol) of 2-chlorobenzyl chloride, and the reaction mixture was heated under reflux for 2 hours. After the reaction mixture had been cooled down to 0° C., 46.4 g (309 mmol) of o-phthalaldehydic acid were added with stirring in the course of about 1 min. Thereafter 135 g (750 mmol) of a 30% strength solution of sodium methylate in methanol were added at 0°-10° C. with stirring in the course of 45 min and stirred in at 0°-10° C. for 3 hours, and the reaction mixture was worked up in a conventional manner to give 72 g (94%) of (E/Z)-2-[2-(2-chlorophenyl)ethenylbenzoic acid in a ratio of ~11:89 in the form of colorless crystals having a melting point of 144°-148° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04857658 |
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| Source dataset | uspto-grants-1989_08 |
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| ORD ID | ord-1f5b93b4561f4c7aab6b23e8d46d015f |
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| Source note | uspto-grants-1989_08 |
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