Sodium sulfate decahydrate → (R)-tert-butyl 1-(4-(hydroxymethyl)oxazol-2-yl)ethylcarbamate

HRID 245939ノート

反応式

HRID 245939 の反応式
C[O:2][C:3]([C:5]1[N:6]=[C:7]([C@H:10]([NH:12][C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH3:11])[O:8][CH:9]=1)=O.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.O.O.O.O.O.O.O.O.O.S([O-])([O-])(=O)=O.[Na+].[Na+]>C1COCC1>[C:16]([O:15][C:13](=[O:14])[NH:12][C@@H:10]([C:7]1[O:8][CH:9]=[C:5]([CH2:3][OH:2])[N:6]=1)[CH3:11])([CH3:17])([CH3:18])[CH3:19]

参加物

5

反応物 3

HCID 62649Sodium sulfate decahydrateHCID 21226445Aluminium lithium hydrideHCID 68671221(R)-methyl 2-(1-(tert-butoxycarbonylamino)ethyl)oxazole-4-carboxylate

生成物 1

HCID 68670262(R)-tert-butyl 1-(4-(hydroxymethyl)oxazol-2-yl)ethylcarbamate収率 103.2%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
0 °C

実験手順

In a round-bottomed flask, 2-((R)-1-tert-butoxycarbonylamino-ethyl)-oxazole-4-carboxylic acid methyl ester (151 mg, 0.56 mmol) was dissolved in THF (4 ml). The pale yellow solution was cooled to 0° C. and lithium aluminum hydride (1.0 M in THF, 0.60 ml, 0.60 mmol) was added dropwise. The reaction mixture was stirred at 0° C. for 1.5 h then sodium sulfate decahydrate was carefully added. When gas evolution had ceased, the ice bath was removed, sodium sulfate was added and the mixture was stirred vigorously for 30 min at room temperature. The suspension was filtered over Celite and rinsed with ethyl acetate/methanol. The filtrate was concentrated to give 140 mg (93%) of [(R)-1-(4-hydroxymethyl-oxazol-2-yl)-ethyl]-carbamic acid tert-butyl ester as yellow oil which was used without further purification.

後処理

  1. customthe ice bath was removed
  2. additionsodium sulfate was added
  3. stirringthe mixture was stirred vigorously for 30 min at room temperature
  4. filtrationThe suspension was filtered over Celite
  5. washrinsed with ethyl acetate/methanol
  6. concentrationThe filtrate was concentrated

出典と根拠

ORDレコード
ord-278991eb5df74b4c81db848bd5717321
出典データセット
uspto-grants-2014_02
特許番号
US08658646B2

反応ノート

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