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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt2-Methyl-2-buteneHCID 10553—
Edukt5-(2,6-Dichloro-4-nitro-phenoxy)-2-methoxy-benzaldehydeHCID 22344863—
EduktSodium ChloriteHCID 23668197—
Lösungsmitteltert-ButanolHCID 6386—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelPotassium Phosphate, TribasicHCID 62657—
Produkt5-(2,6-Dichloro-4-nitro-phenoxy)-2-methoxy-benzoic acidHCID 2234490198,4%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07202275B2
Quelldatensatzuspto-grants-2007_04
ORD IDord-e7a2100a155d4bb2abe9315e6533e9e4
Quellennotizuspto-grants-2007_04