HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453386Generated: October 26, 2026
Tributylamine → 5-(Methoxycarbonyl)-2-methylbenzoic acid
https://huagongshe.com/reaction/453386
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Cesium acetate | HCID 5152919 | — |
| Reactant | Methyl 3-bromo-4-methylbenzoate | HCID 7015747 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(Methoxycarbonyl)-2-methylbenzoic acid | HCID 22999486 | — |
Reaction Steps
A pressure vessel was charged with methyl 3-bromo-4-methylbenzoate (5.0 g, 22 mmol), DMF (20 ml), water (1.25 ml) and tributylamine (8 ml, 34 mmol). Cesium acetate (2.1 g, 11 mmol) was then added and the flask was purged with N2. Palladium acetate (0.25 g, 1.0 mmol) and triphenylphosphine (2.9 g, 11 mmol) were added and the flask was purged with CO gas. The reaction mixture was then heated at 90° C. under 20 psi of CO gas with vigorous stirring overnight. The reaction mixture was diluted with 50 mL of toluene and extracted with saturated NaHCO3 (3×50 ml). The combined aqueous layer was washed with EtOAc (10 mL), then acidified using 2 N HCl to pH 5. The volume was reduced to about 50 mL and the resulting precipitate was collected by filtration, washed with water and dried to give 5-(methoxycarbonyl)-2-methylbenzoic acid as a white solid. MS (ESI, pos. ion) m/z: 193.1 (M−1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492404B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-bb0fa4e87e7a423db7dc22bc87ac3ecb |
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| Source note | uspto-grants-2013_07 |
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