Pyridine → HCID 19818641, compound

HRID 1086932Notes

Reaction equation

HRID 1086932 reaction equation
[C:1](Cl)(=[O:6])[C:2]([O:4][CH3:5])=[O:3].[NH2:8][C:9]1[CH:10]=[C:11]([O:15][CH3:16])[CH:12]=[CH:13][CH:14]=1.N1C=CC=CC=1>C(Cl)Cl>[CH3:16][O:15][C:11]1[CH:10]=[C:9]([NH:8][C:1](=[O:6])[C:2]([O:4][CH3:5])=[O:3])[CH:14]=[CH:13][CH:12]=1

Participants

5

Reactant 3

HCID 1049PyridineHCID 108243-MethoxyanilineHCID 79846Methyl chloroglyoxylate

Product 1

HCID 19818641HCID 19818641, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

A solution of 1.9 ml of methyl chlorooxalate in 10 ml of methylene chloride is added dropwise to a solution of 2.5 g of 3-aminoanisole and 1.5 ml of pyridine in 40 ml of methylene chloride in the course of 10 minutes. After stirring at room temperature for 3 hours, the mixture is poured onto water and extracted with methylene chloride. The extracts are dried over sodium sulfate and evaporated and the residue is crystallised from ether/hexane. Methyl N-(3-methoxyphenyl)-oxamate is obtained.

Workup

  1. additionthe mixture is poured onto water
  2. extractionextracted with methylene chloride
  3. dry with materialThe extracts are dried over sodium sulfate
  4. customevaporated
  5. customthe residue is crystallised from ether/hexane

Sources & evidence

ORD record
ord-3d084b5aafa649b4a8b57fa34e1d5b3f
Source dataset
uspto-grants-1991_07
Patent number
US05032606

Reaction notes

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