Hydrochloric Acid → 4-chloro-1-methyl-1H-pyrrole-2-carboxylic acid

HRID 1802623Notes

Reaction equation

HRID 1802623 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:8]([O:10]C)=[O:9])[N:5]([CH3:7])[CH:6]=1.[OH-].[Na+].Cl>CO>[Cl:1][C:2]1[CH:3]=[C:4]([C:8]([OH:10])=[O:9])[N:5]([CH3:7])[CH:6]=1

Participants

5

Procedure

To a solution of methyl 4-chloro-1-methyl-1H-pyrrole-2-carboxylate (130 mg, 0.75 mmol) in MeOH (4 mL), aq. 1N NaOH (3 mL) was added. After being stirred at room temperature overnight, the mixture was acidified with 1N HCl to pH 1-2. The product was extracted with EtOAc. The EtOAc phase was separated, dried over Na2SO4, concentrated in vacuo to give 4-chloro-1-methyl-1H-pyrrole-2-carboxylic acid as a solid (111 mg).

Workup

  1. extractionThe product was extracted with EtOAc
  2. customThe EtOAc phase was separated
  3. dry with materialdried over Na2SO4
  4. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-298fa2632a1a4da1b37c4f0d03044366
Source dataset
uspto-grants-2013_01
Patent number
US08349873B2

Reaction notes

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