Hydroxylamine → 6-(4-Chlorophenylsulfanyl)-hexa-2,4-dienoic acid hydroxyamide
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]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
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
- distillationdistilled water (9.0 mL)
- additionwas added
- additionthe mixture was made neutral by dropwise addition of concentrated hydrochloric acid (10 M) at 0° C
- extractionThe aqueous solution was extracted with ethyl acetate (3×30 mL)
- dry with materialthe combined extracts were dried over anhydrous MgSO4
- customevaporated to dryness
- 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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