Sodium Hydroxide → HCID 178453623, compound

HRID 271360Notes

Reaction equation

HRID 271360 reaction equation
[C:1]([O:5][C:6]([NH:8][CH2:9][C@@H:10]1[CH2:15][CH2:14][C@H:13]([C:16]([O:18]CCCC)=[O:17])[CH2:12][CH2:11]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[OH-].[Na+]>CO>[C:1]([O:5][C:6]([NH:8][CH2:9][C@@H:10]1[CH2:11][CH2:12][C@H:13]([C:16]([OH:18])=[O:17])[CH2:14][CH2:15]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]

Participants

4

Procedure

To a solution of crude butyl cis-4-{[(tert-butoxycarbonyl)amino]methyl}cyclohexanecarboxylate (28.4 g, approximately 79.3 mmol) in methanol (200 ml) was added dropwise over five minutes 2N sodium hydroxide solution (400 mmol). The mixture was stirred 18 hours at ambient temperature under nitrogen. The mixture was concentrated under reduced pressure to remove methanol. To the aqueous residue was added methyl orange (1 mg) and 3N hydrochloric acid was added to adjust the mixture to pH 4. The mixture was extracted with ethyl acetate (3×200 ml). The extract was washed with water (100 ml), and brine (100 ml), dried (sodium sulfate), filtered, and the solvent evaporated under reduced pressure to give cis-4-{[(tert-butoxycarbonyl)amino]methyl}cyclohexanecarboxylic acid (18.76 g, 92%) as an off-white solid. MS: 258.3 (M+1).

Workup

  1. concentrationThe mixture was concentrated under reduced pressure
  2. customto remove methanol
  3. additionTo the aqueous residue was added methyl orange (1 mg) and 3N hydrochloric acid
  4. additionwas added
  5. extractionThe mixture was extracted with ethyl acetate (3×200 ml)
  6. washThe extract was washed with water (100 ml), and brine (100 ml)
  7. dry with materialdried (sodium sulfate)
  8. filtrationfiltered
  9. customthe solvent evaporated under reduced pressure

Sources & evidence

ORD record
ord-021e51cbf7c3496aac3d8fd3f88ad31f
Source dataset
uspto-grants-2008_11
Patent number
US07452893B2

Reaction notes

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