HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1372644Erstellt: 25. Oktober 2026
5-Fluoro-o-tolyl Isothiocyanate → Methyl (2-(5-fluoro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetate
https://huagongshe.com/reaction/1372644
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 5-Fluoro-o-tolyl Isothiocyanate | HCID 519443 | — |
| Edukt | Methyl (4-amino-2-fluoro-3-hydroxyphenyl)acetate | HCID 17859032 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | Methyl (2-(5-fluoro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetate | HCID 44607521 | 56% |
Reaktionsschritte
In methanol (30 ml) was dissolved methyl (4-amino-2-fluoro-3-hydroxyphenyl)acetate (1.0 g, 5.02 mmol). To the resulting solution was added 5-fluoro-2-methylphenyl isothiocyanate (1.0 g, 5.98 mmol). After the resulting mixture was stirred at room temperature for 5 days, mercuric oxide (yellow) (1.14 g, 4.36 mmol) was added thereto. The mixture was stirred at 70° C. for 6 hours. After cooling to room temperature, the reaction mixture was filtered through Celite and washed with methanol. The filtrate was distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from chloroform/ethyl acetate (30/1, v/v) eluate fractions, methyl (2-(5-fluoro-2-methylphenylamino)-7-fluoro-6-benzoxazolyl)acetate (810 mg, 56% (2 steps)) was obtained as a pink solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07157487B2 |
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| Quelldatensatz | uspto-grants-2007_01 |
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| ORD ID | ord-672c550ec85c4431afa5341f70e99fc0 |
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| Quellennotiz | uspto-grants-2007_01 |
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