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

HRID 1895484Notes

Reaction equation

HRID 1895484 reaction equation
[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]

Participants

5

Reactant 2

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

Product 1

HCID 858681944-Amino-3-chloro-2-fluoro-5-nitro-benzoic acid methyl esterYield 39.4%

Reagents, catalysts & solvents 2

HCID 887MethanolSolventHCID 8028TetrahydrofuranSolvent

Procedure

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.

Workup

  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

Sources & evidence

ORD record
ord-71738c1932ac470b858d5c3c49fb936e
Source dataset
uspto-grants-2013_08
Patent number
US08513293B2

Reaction notes

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