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Hydroxylamine → 6-(4-Dimethylaminophenylsulfinyl)hexanoic acid hydroxamide

HRID 2245796
ノート
印刷プレビュー

反応式

HRID 2245796 の反応式
C[O:2][C:3](=O)[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][S:9]([C:11]1[CH:16]=[CH:15][C:14]([N:17]([CH3:19])[CH3:18])=[CH:13][CH:12]=1)=[O:10].[NH2:21][OH:22].[OH-].[K+].CO>C1COCC1>[OH:22][NH:21][C:3](=[O:2])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][S:9]([C:11]1[CH:16]=[CH:15][C:14]([N:17]([CH3:19])[CH3:18])=[CH:13][CH:12]=1)=[O:10]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 787HydroxylamineHCID 887MethanolHCID 14797Potassium HydroxideHCID 100175446-(4-Dimethylamino-benzenesulfinyl)-hexanoic acid methyl ester

生成物 1

HCID 103573496-(4-Dimethylaminophenylsulfinyl)hexanoic acid hydroxamide収率 61%

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒

反応条件

温度
0 °C

実験手順

To a solution of the 6-(4-dimethylamino-benzenesulfinyl)-hexanoic acid methyl ester (1.2 g, 4.0 mmol) in distilled THF (30 mL) containing 50% aqueous hydroxylamine (2.65 mL, 40 mmol) was added at 0° C. a solution of potassium hydroxide in methanol (6.8 mL, 1M, 6.8 mmol) in a dropwise manner. After stirring at 0° C. for 1 h, distilled water (30 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 (3×50 mL) and the combined extracts were washed with brine (100 mL), dried over anhydrous MgSO4, filtered and evaporated to dryness. The solid residue was recrystallised from acetone to give the title compound (728 mg, 61%) as a white powder, mp 95-97° C.

後処理

  1. distillationdistilled water (30 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 (3×50 mL)
  5. washthe combined extracts were washed with brine (100 mL)
  6. dry with materialdried over anhydrous MgSO4
  7. filtrationfiltered
  8. customevaporated to dryness
  9. customThe solid residue was recrystallised from acetone

出典と根拠

ORDレコード
ord-42898a06a45249aca04b631d4a735f6f
出典データセット
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07683185B2

反応ノート

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