HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 507026Erstellt: 25. Oktober 2026
Iodine → Methyl 2-amino-5-iodo-4-(trifluoromethyl)benzoate
https://huagongshe.com/reaction/507026
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Iodine | HCID 807 | — |
| Edukt | Methyl 2-Amino-4-(trifluoromethyl)benzoate | HCID 12601886 | — |
| Katalysator | HCID 178418844 | HCID 178418844 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Methyl 2-amino-5-iodo-4-(trifluoromethyl)benzoate | HCID 53436880 | 99% |
Reaktionsschritte
Add a solution of methyl 2-amino-4-trifluoromethylbenzoate (178 g, 812 mmol) in ethanol (3.3 L) to a suspension of iodine (206.1 g, 812 mmol) and silver (II) sulfate (253 g, 812 mmol) in ethanol (5 L) at room temperature under an atmosphere of nitrogen and stir for 2 h. Filter the suspension through a pad of a Celite®, wash the pad with additional ethanol (2 L) and remove the solvents from the combined filtrates under reduced pressure at 40° C. Dissolve the residue in ethyl acetate (7.5 L) and wash with saturated sodium bicarbonate solution (3×1.5 L), water (3×1.5 L) and brine (2 L). Dry the organic phase over anhydrous magnesium sulfate, filter and remove the solvent under reduced pressure to give the title compound as a pale brown crystalline solid (276.0 g, 99%). 1H NMR (300 MHz, CDCl3) δ 8.39 (1H, s), 6.99 (1H, s), 5.93 (2H, s), 3.90 (3 H, s).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07786108B2 |
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| Quelldatensatz | uspto-grants-2010_08 |
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| ORD ID | ord-fe593709d9aa4b6c9596f60987a1d004 |
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| Quellennotiz | uspto-grants-2010_08 |
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