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Hydrochloric Acid → (S)-4-(t-Butyldimethylsilyloxy)pyrrolidin-2-one

HRID 1517206
ノート
印刷プレビュー

反応式

HRID 1517206 の反応式
N1C=CN=C1.[Si:6](Cl)([C:9]([CH3:12])([CH3:11])[CH3:10])([CH3:8])[CH3:7].[OH:14][C@@H:15]1[CH2:19][NH:18][C:17](=[O:20])[CH2:16]1.Cl>CN(C)C=O>[C:9]([Si:6]([CH3:8])([CH3:7])[O:14][C@@H:15]1[CH2:19][NH:18][C:17](=[O:20])[CH2:16]1)([CH3:12])([CH3:11])[CH3:10]
参加物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 313Hydrochloric AcidHCID 795ImidazoleHCID 28928tert-Butyldimethylsilyl chlorideHCID 1550842-Pyrrolidinone, 4-hydroxy-, (4S)-

生成物 1

HCID 11074789(S)-4-(t-Butyldimethylsilyloxy)pyrrolidin-2-one収率 100.9%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide
溶媒

実験手順

Imidazole (93.73 g, 1.26 mol) and tert-butyldimethylsilyl chloride (145.3 g, 0.96 mol) were added to a solution of (S)-4-hydroxy-2-pyrrolidone (92.8 g, 0.92 mol) in dimethylformamide (560 mL). The mixture was then stirred at room temperature for 16 hours, after which time it was poured over ice and an aqueous solution of hydrochloric acid (0.2 M, 300 mL) was added. The mixture was stirred at room temperature for 10 minutes, and then extracted with ethyl acetate (4×500 mL). The combined organic extracts were washed with brine (1000 mL), dried over sodium sulphate, filtered, and evaporated under reduced pressure to give (S)-4-(tert-butyl-dimethyl-silanyloxy)-pyrrolidin-2-one as a solid (200 g, 100%).

後処理

  1. additionafter which time it was poured over ice
  2. stirringThe mixture was stirred at room temperature for 10 minutes
  3. extractionextracted with ethyl acetate (4×500 mL)
  4. washThe combined organic extracts were washed with brine (1000 mL)
  5. dry with materialdried over sodium sulphate
  6. filtrationfiltered
  7. customevaporated under reduced pressure

出典と根拠

ORDレコード
ord-4c427f98e4d84461943f225f02e56048
出典データセット
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08232269B2

反応ノート

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