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tert-Butylsulfinamide, (S)-(-)- → tert-butyl 3-[2-[(E)-[(S)-tert-butylsulfinyl]iminomethyl]-3-methylphenyl]propanoate

HRID 64426
ノート
印刷プレビュー

反応式

HRID 64426 の反応式
[CH:1]([C:3]1[C:8]([CH3:9])=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:10][CH2:11][C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])=O.[CH3:19][C:20]([S@@:23]([NH2:25])=[O:24])([CH3:22])[CH3:21]>C1COCC1.CCO.CCO.CCO.CCO.[Ti]>[C:20]([S@@:23](/[N:25]=[CH:1]/[C:3]1[C:8]([CH3:9])=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:10][CH2:11][C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])=[O:24])([CH3:22])([CH3:21])[CH3:19]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 11355477tert-Butylsulfinamide, (S)-(-)-HCID 86713435Tert-butyl 3-(2-formyl-3-methylphenyl)propanoate

生成物 1

HCID 90072800tert-butyl 3-[2-[(E)-[(S)-tert-butylsulfinyl]iminomethyl]-3-methylphenyl]propanoate収率 77.8%

試薬・触媒・溶媒 2

HCID 2724286Titanium(IV)ethoxide触媒HCID 8028Tetrahydrofuran溶媒

実験手順

To a solution of 305 mg of tert-butyl 3-(2-formyl-3-methylphenyl)propanoate in 3 ml of THF 3 ml were added 298 mg of (S)-2-methyl-2-propanesulfinamide and 0.62 ml of tetraethyl orthotitanate, followed by stirring at room temperature for 16 hours. The reaction mixture was poured into ice water and the insoluble material was filtered through Celite. To the filtrate was added chloroform to carry out a layer separation operation. The organic layer was washed with water and subsequentially with saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 336 mg of tert-butyl 3-{2-[(E)-{[(S)-tert-butylsulfinyl]imino}methyl]-3-methylphenyl}propanoate.

後処理

  1. filtrationthe insoluble material was filtered through Celite
  2. additionTo the filtrate was added chloroform
  3. customa layer separation operation
  4. washThe organic layer was washed with water and subsequentially with saturated brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customthe solvent was evaporated under reduced pressure
  7. customThe obtained residue was purified by silica gel column chromatography

出典と根拠

ORDレコード
ord-2acaaa5049f34efc927e8517584e58cd
出典データセット
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09447090B2

反応ノート

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