Hydrochloric Acid → HCID 86608551, compound

HRID 2245803Notes

Reaction equation

HRID 2245803 reaction equation
C([O:3][C:4](=[O:21])/[CH:5]=[CH:6]/[CH:7]=[CH:8]/[C:9]1[S:13][C:12]2[CH:14]=[CH:15][C:16]([N:18]([CH3:20])[CH3:19])=[CH:17][C:11]=2[CH:10]=1)C.NO.[OH-].[K+].CO.Cl>C1COCC1.O>[CH3:20][N:18]([CH3:19])[C:16]1[CH:15]=[CH:14][C:12]2[S:13][C:9](/[CH:8]=[CH:7]/[CH:6]=[CH:5]/[C:4]([OH:21])=[O:3])=[CH:10][C:11]=2[CH:17]=1

Participants

8

Conditions

Temperature
20 °C

Procedure

To a solution of (2E,4E)-5-(5-dimethylaminobenzo[b]thiophen-2-yl)-penta-2,4-dienoic acid ethyl ester (540 mg, 1.8 mmol) in dry THF (10 mL) was added at 0° C. an aqueous solution of hydroxylamine (50%, 1.1 mL, 16.6 mmol). To this mixture was added a solution of potassium hydroxide in methanol (2.9 mL, 1M, 2.9 mmol) over a period of 40 minutes at 0° C. The mixture was stirred at 20° C. for 2 hours, and water (10 mL) was then added. The solution was acidified to pH 5 by addition of concentrated hydrochloric acid (10 M, CAUTION), then extracted with ethyl acetate (50 mL). The organic layer was washed with brine (25 mL), dried over anhydrous MgSO4, filtered and concentrated under reduced pressure to give a solid which was recrystallised from ethanol to give the title compound (367 mg, 71%) as an orange solid, mp 195° C. (decomp.).

Workup

  1. extractionextracted with ethyl acetate (50 mL)
  2. washThe organic layer was washed with brine (25 mL)
  3. dry with materialdried over anhydrous MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. customto give a solid which
  7. customwas recrystallised from ethanol

Sources & evidence

ORD record
ord-9819196358eb460199dded3e0de0005a
Source dataset
uspto-grants-2010_03
Patent number
US07683185B2

Reaction notes

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