Trimethylsilyldiazomethane → 4-Amino-3-chloro-2-fluoro-5-nitro-benzoic acid methyl ester

HRID 217069Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 217069
[NH2:1][C:2]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4]([F:14])[C:3]=1[Cl:15].[Si](C=[N+]=[N-])(C)(C)[CH3:17]>C1COCC1.CO>[CH3:17][O:7][C:6](=[O:8])[C:5]1[CH:9]=[C:10]([N+:11]([O-:13])=[O:12])[C:2]([NH2:1])=[C:3]([Cl:15])[C:4]=1[F:14]

Komponenten

5

Edukt 2

HCID 167693TrimethylsilyldiazomethaneHCID 211141824-Amino-3-chloro-2-fluoro-5-nitro-benzoic acid

Produkt 1

HCID 858681944-Amino-3-chloro-2-fluoro-5-nitro-benzoic acid methyl esterAusbeute 39,4 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887MethanolLösungsmittelHCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a stirred solution of 4-amino-3-chloro-2-fluoro-5-nitro-benzoic acid 3a (3.61 g, 15.4 mmol) in THF (30 mL) and MeOH (10 mL), TMS diazomethane (9.23 mL, 2.0 M solution in hexanes, 18.5 mmol) is added. After completion of reaction, the reaction mixture is concentrated via rotary evaporation with acetic acid in the trap. The recovered oily solid is triturated with diethyl ether to provide 1.51 g of a yellow solid. The filtrate is concentrated and triturated with diethyl ether to give an additional 0.69 g of yellow solid. A total of 2.20 g (57%) of pure desired product is recovered.

Aufarbeitung

  1. customAfter completion of reaction
  2. concentrationthe reaction mixture is concentrated via rotary evaporation with acetic acid in the trap
  3. customThe recovered oily solid is triturated with diethyl ether

Quellen und Nachweise

ORD-Eintrag
ord-a2425dd159b845498503a9c6ac7e2d83
Quelldatensatz
uspto-grants-2012_06
Patentnummer
US08193231B2

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