Acetic Acid → Methyl 4-formamido-3-methoxybenzoate

HRID 1362587Notes

Reaction equation

HRID 1362587 reaction equation
[C:1](O)(=[O:3])C.C(O)=O.C1COCC1.[CH3:13][O:14][C:15](=[O:25])[C:16]1[CH:21]=[CH:20][C:19]([NH2:22])=[C:18]([O:23][CH3:24])[CH:17]=1>O>[CH3:13][O:14][C:15](=[O:25])[C:16]1[CH:21]=[CH:20][C:19]([NH:22][CH:1]=[O:3])=[C:18]([O:23][CH3:24])[CH:17]=1

Participants

6

Reactant 4

HCID 176Acetic AcidHCID 284Formic AcidHCID 8028TetrahydrofuranHCID 602411Methyl 4-amino-3-methoxybenzoate

Product 1

HCID 23085082Methyl 4-formamido-3-methoxybenzoate

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

Anhydrous acetic acid (268 mL) was added dropwise to formic acid (401 mL) at room temperature, and the reaction solution was agitated for 40 minutes at room temperature. To this reaction solution, a THF (600 mL) solution of 4-amino-3-methoxybenzoic acid methyl ester (134 g) was added dropwise at room temperature, and the reaction solution was agitated for 1 hour. 3.8 L of iced water was added to the reaction solution, and the deposited solids were separated by filtering, and further washed with water (2 L). 111 g of the title compound was obtained by drying the obtained solid at 50° C. overnight. The physical properties was in agreement with the reported values (CAS#700834-18-0).

Workup

  1. stirringthe reaction solution was agitated for 1 hour
  2. customthe deposited solids were separated
  3. filtrationby filtering
  4. washfurther washed with water (2 L)

Sources & evidence

ORD record
ord-e1c2854509d64194a94031e63564637a
Source dataset
uspto-grants-2011_02
Patent number
US07880009B2

Reaction notes

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