HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1270580Erstellt: 25. Oktober 2026
Hydrochloric Acid → 5-(2,6-Dichloro-4-nitro-phenoxy)-2-methoxy-benzoic acid
https://huagongshe.com/reaction/1270580
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 2-Methyl-2-butene | HCID 10553 | — |
| Edukt | 5-(2,6-Dichloro-4-nitro-phenoxy)-2-methoxy-benzaldehyde | HCID 22344863 | — |
| Edukt | Sodium Chlorite | HCID 23668197 | — |
| Lösungsmittel | tert-Butanol | HCID 6386 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Produkt | 5-(2,6-Dichloro-4-nitro-phenoxy)-2-methoxy-benzoic acid | HCID 22344901 | 98,4% |
Reaktionsschritte
To a solution of 5-(2,6-dichloro-4-nitro-phenoxy)-2-methoxy-benzaldehyde (3.0 g, 8.8 mmol) in a mixture of THF (50 ml), tert-butyl alcohol (50 ml) and 2-methyl-2-butene (11 ml, 132 mmol) was added dropwise a solution of sodium chlorite (7.1 g, 79 mmol) in potassium phosphate buffer (100 ml of a 0.6 M solution, 60 mmol). The resulting mixture was stirred vigorously for 16 h at RT then acidified with 1 M HCl (200 ml). The resulting mixture was extracted with EtOAC (3×150 ml). The combined EtOAc extracts were washed with 1 M HCl (2×250 ml), water (250 ml), 10% NaHSO3, and brine (250 ml). The extracts were dried (Na2SO4), filtered, and concentrated to give the title compound of Step B (3.1 g) as a yellow solid. The title product of Step B was used in the next step without further purification. MS (ES−) Calc.: 357.0, Found: 356.0 (M−1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07202275B2 |
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| Quelldatensatz | uspto-grants-2007_04 |
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| ORD ID | ord-e7a2100a155d4bb2abe9315e6533e9e4 |
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| Quellennotiz | uspto-grants-2007_04 |
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