HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270050Generated: October 25, 2026
Monomethyl terephthalate → 2-(4-Methoxycarbonylbenzamido)-4'-methoxyacetophenone
https://huagongshe.com/reaction/2270050
Participants
| Role | Name | HCID | Charge |
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| Reactant | Monomethyl terephthalate | HCID 15513 | — |
| Reactant | 2-Amino-4'-methoxyacetophenone hydrochloride | HCID 12487188 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-(4-Methoxycarbonylbenzamido)-4'-methoxyacetophenone | HCID 13640369 | 92.1% |
Reaction Steps
To a solution of 2-amino-4′-methoxyacetophenone hydrochloride (5.33 g) in pyridine (4.28 ml), triethylamine (3.68 ml) and dichloromethane (50 ml) was added dropwise a solution of terephthalic acid monomethyl ester (5.25 g) in dichloromethane (10 ml) at 0° C. The reaction mixture was allowed to warm to room temperature, and stirred for 3 hours. To the reaction mixture was added dichloromethane (200 ml), washed with 1N-sodium hydroxide (100 ml×2), saturated hydrogen carbonate aqueous solution (100 ml×2) and brine, and dried over magnesium sulfate. Magnesium sulfate was filtered off, and the filtrate was evaporated under reduced pressure. The solids were slurried in n-hexane, and collected by filtration to give 2-(4-methoxycarbonyl-benzamido)-4′-methoxyacetophenone (7.97 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06331521B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-6166f9853aa6469cbc73aef21e32c70a |
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| Source note | uspto-grants-2001_12 |
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