Benzyl Bromide → Ethyl 3-oxo-5-phenylpentanoate

HRID 3396

反応式

HRID 3396 の反応式
[H-].[Na+].[C:3]([O:9][CH2:10][CH3:11])(=[O:8])[CH2:4][C:5]([CH3:7])=[O:6].[CH2:12](Br)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>CCCCCC.C1COCC1>[CH2:10]([O:9][C:3](=[O:8])[CH2:4][C:5]([CH2:7][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:6])[CH3:11]

参加物

6

反応条件

温度
-10 °C

実験手順

NaH (13.8 g, 0.6 mole) was washed twice with hexane (2×50 ml) and suspended in 250 ml of freshly distilled THF. Next ethyl acetoacetate (75 ml, excess) was added dropwise carefully while the receiving flask was cooled at -10° C. After the addition was complete, it was stirred at -10° C. for 2 hours and at room temperature for 30 min. Benzylbromide (51.0 g, 0.3 mole) in THF was added dropwise at room temperature to the above solution. The reaction mixture was stirred overnight at room temperature. The reaction was terminated the next day by pouring into ice cold water, brought to neutral pH, and extracted with ether/ethylacetate. The combined ether/ethylacetate extracts were rinsed over brine and dried over Na2SO4. Removal of the solvent followed by careful vacuum distillation gave ethyl-benzylacetoacetate, bp 276° C. IR: (neat), cm-1 : 2900-3050, 1690-1760 (broad), 1655. NMR (CDCl3):δ:1.25 (t1 3H, CH2CH3); 2.25 (s, 3H, COCH3); 3.20 (d, 2H, benzylic CH2); 3.8 (t, 1H, COCHCO); 4.20 (q, 2H, OCH2CH3); 7.15-7.35 (m, 5H, Ar-H).

後処理

  1. additionAfter the addition
  2. stirringThe reaction mixture was stirred overnight at room temperature
  3. customThe reaction was terminated the next day
  4. additionby pouring into ice cold water
  5. extractionextracted with ether/ethylacetate
  6. washThe combined ether/ethylacetate extracts were rinsed over brine
  7. dry with materialdried over Na2SO4
  8. customRemoval of the solvent
  9. distillationfollowed by careful vacuum distillation

出典と根拠

ORDレコード
ord-123a12fd08654e45b37f1f604736d38c
出典データセット
uspto-grants-1998_03
特許番号
US05733934

関連ノート

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