HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 240801Generated: October 29, 2026
4-Methoxybenzoic Acid → HCID 67079010, compound
https://huagongshe.com/reaction/240801
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methoxybenzoic Acid | HCID 7478 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 86664626 | HCID 86664626 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67079010 | HCID 67079010 | 420.5% |
Reaction Steps
Under a nitrogen atmosphere, a catalytic amount of dimethylformamide was added to a solution of p-methoxybenzoic acid (5 g, 33.0 mmol) in dichloromethane (50 mL), and the obtained mixture was then cooled to 0° C. Thereafter, oxalyl chloride (5.8 mL, 66.1 mmol) was added to the reaction solution, and the obtained mixture was then stirred at room temperature for 30 minutes. Thereafter, the solvent was distilled away, and the obtained residue was then added to a solution of 5-aminolevulinic acid methyl hydrochloride (1.0 g, 5.50 mmol) and triethylamine (2.3 mL, 16.5 mmol) in dichloromethane (80 mL) that had been cooled to 0° C. under a nitrogen atmosphere. The obtained mixture was stirred at room temperature for 3 hours. Thereafter, the solvent was distilled away, and the obtained residue was then purified by silica gel column chromatography (hexane/ethyl acetate), so as to obtain the title compound (6.46 g, yield: 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08648103B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-dfa45e8e97d347cda520d7b2e7ed073f |
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| Source note | uspto-grants-2014_02 |
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