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

HRID 2245761
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HRID 2245761 반응식
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
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참가 물질

6

반응물 4

HCID 787HydroxylamineHCID 887MethanolHCID 14797Potassium HydroxideHCID 859734646-(4-Chlorophenylsulfanyl)-hexa-2,4-dienoic acid methyl ester

생성물 1

HCID 573528496-(4-Chlorophenylsulfanyl)-hexa-2,4-dienoic acid hydroxyamide수율 48%

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매

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온도
0 °C

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-8dd72fe8a47b4265ad30ae66e65a1df6
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07683185B2

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