Acetic Acid → 1-(6-Benzyloxycarbonylamino-hexanoyl)-4-oxo-pyrrolidine-3-carboxylic Acid Ethyl Ester

HRID 1893034

反応式

HRID 1893034 の反応式
CC(C)([O-])C.[K+].[CH2:7]([O:9][C:10](=[O:38])[CH2:11][CH2:12][N:13]([C:20](=[O:37])[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][NH:26][C:27]([O:29][CH2:30][C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=1)=[O:28])[CH2:14][C:15](OCC)=[O:16])[CH3:8].C(O)(=O)C>C1(C)C=CC=CC=1>[CH2:7]([O:9][C:10]([CH:11]1[C:15](=[O:16])[CH2:14][N:13]([C:20](=[O:37])[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][NH:26][C:27]([O:29][CH2:30][C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)=[O:28])[CH2:12]1)=[O:38])[CH3:8]

参加物

5

反応条件

温度
0 °C

実験手順

To a suspension of potassium t-butoxide (7.12 g, 64 mmol) in toluene (150 mL) at 0° C. under nitrogen, was added diester 59 (20 g, 44 mmol) in toluene (25 mL) over a 10 min period. The solution was stirred for 30 min at 0° C. and 5 mL of glacial acetic acid was added, immediately followed by 25 g of NaH2PO4.H2O in 250 mL of ice-cold water. The resultant mixture was extracted with chloroform (3×200 mL), and the combined organic extracts were washed twice with phosphate buffer (2×25 mL, pH=7.0), dried over anhydrous sodium sulfate and evaporated to dryness. The residue was dissolved in toluene (300 mL), cooled to 0° C., and extracted with cold pH 9.5 carbonate buffer (3×150 mL). The aqueous extracts were converted to pH 3 with phosphoric acid, and extracted with chloroform (5×125 mL) which were combined, dried, and evaporated to a afford keto ester 60 (12 g, 45%).

後処理

  1. extractionThe resultant mixture was extracted with chloroform (3×200 mL)
  2. washthe combined organic extracts were washed twice with phosphate buffer (2×25 mL, pH=7.0)
  3. dry with materialdried over anhydrous sodium sulfate
  4. customevaporated to dryness
  5. dissolutionThe residue was dissolved in toluene (300 mL)
  6. temperaturecooled to 0° C.
  7. extractionextracted with cold pH 9.5 carbonate buffer (3×150 mL)
  8. extractionextracted with chloroform (5×125 mL) which
  9. customdried
  10. customevaporated to a afford keto ester 60 (12 g, 45%)

出典と根拠

ORDレコード
ord-57f4e485299a4cfb94c6e056ab9c8389
出典データセット
uspto-grants-2013_08
特許番号
US08507661B2

関連ノート

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