Sodium Hydroxide → 4-Cyano-5-morpholin-4-ylthiophene-2-carboxylic acid

HRID 1615509Notes

Reaction equation

HRID 1615509 reaction equation
[C:1]([C:3]1[CH:4]=[C:5]([C:14]([O:16]CC)=[O:15])[S:6][C:7]=1[N:8]1[CH2:13][CH2:12][O:11][CH2:10][CH2:9]1)#[N:2].[OH-].[Na+]>C1COCC1.CO.O>[C:1]([C:3]1[CH:4]=[C:5]([C:14]([OH:16])=[O:15])[S:6][C:7]=1[N:8]1[CH2:13][CH2:12][O:11][CH2:10][CH2:9]1)#[N:2]

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 68629708Ethyl 4-cyano-5-morpholin-4-ylthiophene-2-carboxylate

Product 1

HCID 686278674-Cyano-5-morpholin-4-ylthiophene-2-carboxylic acidYield 88%

Reagents, catalysts & solvents 1

HCID 21892291Methanol tetrahydrofuran waterSolvent

Procedure

To a solution of ethyl 4-cyano-5-morpholin-4-ylthiophene-2-carboxylate (0.06 g, 0.23 mmol) in THF/MeOH/water (3:1:1) (5 mL) was added sodium hydroxide (0.095 g, 2.3 mmol). The reaction mixture was allowed to stir at rt for 20 h and was concentrated. The residue was acidified to pH 1-2 with 1N HCl and was extracted with EtOAc. The organic solutions were combined, washed with brine, dried over MgSO4, filtered and concentrated to give the title compound (0.048 g, 88%). LCMS: (FA) ES+ 239.1. 1H NMR (400 MHz, d6-DMSO) δ:7.67 (s, 1H), 3.72-3.75 (m, 4H) and 3.52-3.55 (m, 4H).

Workup

  1. concentrationwas concentrated
  2. extractionwas extracted with EtOAc
  3. washwashed with brine
  4. dry with materialdried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-27a96d5fc0e743fda9073848c0c33ed5
Source dataset
uspto-grants-2014_07
Patent number
US08765746B2

Reaction notes

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