HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 480672Erstellt: 23. Oktober 2026
4-Methylbenzoyl Chloride → Dimethyl 5-[(4-methylbenzoyl)amino]isophthalate
https://huagongshe.com/de/reaction/480672
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Methylbenzoyl Chloride | HCID 13405 | — |
| Edukt | Dimethyl 5-aminoisophthalate | HCID 66831 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | Dimethyl 5-[(4-methylbenzoyl)amino]isophthalate | HCID 721197 | 99% |
Reaktionsschritte
To 1.20 g (5.74 mmol) of methyl 5-amino-3-(methoxycarbonyl)benzoate, compound 87, suspended in 50 mL of chloroform and 1.05 mL (6.00 mmol) of diisopropylethylamine was added 836 μL (6.32 mmol) of p-toluoyl chloride in 10 mL of chloroform over 30 min. The reaction was allowed to stir at ambient temperature for 2 hr. Then, another 100 μL (0.60 mmol) of diisopropylethylamine and 100 μL (0.76 mmol) of p-toluoyl chloride in 2 mL of chloroform was added. After an addition 30 min, the volatiles were removed by rotary evaporation and the resulting residue was dissolved in ethyl acetate and extracted with 0.1 N aqueous NaOH followed by extraction with water. The organic layer was dried (MgSO4), filtered, and volatiles removed in vacuo. This provided 1.86 g (5.68 mmol) of the desired compound. The product was identified by 1H NMR and mass spectroscopy and purity was assessed by RP-HPLC.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06653321B1 |
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| Quelldatensatz | uspto-grants-2003_11 |
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| ORD ID | ord-4dc31118c93f4d6299c5f6ab2af4819d |
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| Quellennotiz | uspto-grants-2003_11 |
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