Hydroxylamine → 6-(4-Chlorophenylsulfanyl)-hexa-2,4-dienoic acid hydroxyamide

HRID 2245761Notes

Reaction equation

HRID 2245761 reaction equation
C[O:2][C:3](=O)[CH:4]=[CH:5][CH:6]=[CH:7][CH2:8][S:9][C:10]1[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][CH:11]=1.[NH2:18][OH:19].[OH-].[K+].CO>C1COCC1>[OH:19][NH:18][C:3](=[O:2])[CH:4]=[CH:5][CH:6]=[CH:7][CH2:8][S:9][C:10]1[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][CH:11]=1

Participants

6

Conditions

Temperature
0 °C

Procedure

To a solution of the 6-(4-chlorophenylsulfanyl)-hexa-2,4-dienoic acid methyl ester (0.44 g, 1.64 mmol) in distilled THF (9.0 mL) containing 50% aqueous hydroxylamine (1.0 ml, 15.2 mmol) was added at 0° C. a solution of potassium hydroxide in methanol (1M, 2.6 mL, 2.6 mmol) over a period of 30 minutes. After stirring at 0° C. for 1 h, distilled water (9.0 mL) was added and the mixture was made neutral by dropwise addition of concentrated hydrochloric acid (10 M) at 0° C. The aqueous solution was extracted with ethyl acetate (3×30 mL) and the combined extracts were dried over anhydrous MgSO4, and evaporated to dryness. The residue was recrystallised from acetone to give the title compound (0.21 g, 48%) as a pale brown powder, mp 120-122° C. (decomp).

Workup

  1. distillationdistilled water (9.0 mL)
  2. additionwas added
  3. additionthe mixture was made neutral by dropwise addition of concentrated hydrochloric acid (10 M) at 0° C
  4. extractionThe aqueous solution was extracted with ethyl acetate (3×30 mL)
  5. dry with materialthe combined extracts were dried over anhydrous MgSO4
  6. customevaporated to dryness
  7. customThe residue was recrystallised from acetone

Sources & evidence

ORD record
ord-8dd72fe8a47b4265ad30ae66e65a1df6
Source dataset
uspto-grants-2010_03
Patent number
US07683185B2

Reaction notes

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