HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2284830Generated: October 31, 2026
3-Methoxybenzoic Acid → (3-Methoxyphenyl)(phenyl)methanone
https://huagongshe.com/reaction/2284830
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Methoxybenzoic Acid | HCID 11461 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (3-Methoxyphenyl)(phenyl)methanone | HCID 12451863 | 151.5% |
Reaction Steps
To the mixture of phosphorus pentachloride (3763 g, 18.1 mol) in 7.5 L of benzene, 3-methoxy benzoic acid (2500 g, 16.4 mol) was added in portions. The mixture was stirred for 50 minutes until it became homogenous. The formation of the acid chloride was controlled by TLC. After completion, the mixture was cooled down to 10° C., reactor was covered with aluminum foil and aluminium trichloride (4820 g, 36.1 mol) was added in portions (internal temperature was held up to 30° C. maximum). Stirring was continued for 18 hours at RT. The reaction was monitored by TLC (AcOEt:hex 1:9). After completion, the reaction mixture was poured into ice and was diluted with AcOEt (7 L). Then organic layer was separated and the aqueous layer was extracted with AcOEt (2×10 L, 1×6 L). The combined organic layers were washed with water (5×3 L) to pH-6-7, saturated aqueous sodium hydrogen carbonate solution (15 L), dried (sodium sulfate), filtered and the solvent evaporated at reduced pressure to give a crude oil. The product was purified by vacuum distillation (130-139° C., 2 mbar) to obtain title compound (2637 g, 76%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145409B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-e34b2b4e18504979a824c6f96ecb08fb |
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| Source note | uspto-grants-2015_09 |
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