Ethyl formate → rac. 4-Benzyloxy-3-methylbutanal

HRID 1277532ノート

反応式

HRID 1277532 の反応式
[CH2:1]([O:8][CH2:9][CH:10]([CH3:14])[CH2:11][C:12]#N)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].C([Al+]CC(C)C)C(C)C.C(OCC)=[O:26].[Cl-].[NH4+]>C1(C)C=CC=CC=1.CCCCCC>[CH2:1]([O:8][CH2:9][CH:10]([CH3:14])[CH2:11][CH:12]=[O:26])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

参加物

7

実験手順

A solution of 5.8 g. (0.0307 mole) of rac. 4-benzyloxy-3-methylbutyronitrile in 290 ml. of hexane was stirred at -65° C. to -70° C. while 22.4 ml. (4.78 g.; 0.0337 mole) of 25% diisobutylaluminum hydride solution in toluene was added dropwise. Theresulting solution was stirred at -65° C. to -70° C. for 0.5 hours then at room temperature for 5 hours whereupon 2.8 ml. of ethyl formate was added dropwise. The reaction mixture was then treated with 250ml. of saturated aqueous ammonium chloride solution. Stirring was continuedfor 20 minutes at which point 125 ml. of 5% by weight aqueous sulfuric acidwas added and stirring was continued for an additional 10 minutes. The organic layer was separated and the aqueous layer was extracted with ether. The organic solutions were combined and processed as in Example 1 giving 4.79 g. (81.3%) of rac. 4-benzyloxy-3-methylbutanal as a yellow oil.

後処理

  1. waitat room temperature for 5 hours whereupon 2.8 ml
  2. additionThe reaction mixture was then treated with 250ml
  3. stirringStirring
  4. waitwas continuedfor 20 minutes at which
  5. additionof 5% by weight aqueous sulfuric acidwas added
  6. stirringstirring
  7. waitwas continued for an additional 10 minutes
  8. customThe organic layer was separated
  9. extractionthe aqueous layer was extracted with ether

出典と根拠

ORDレコード
ord-ee60592bf1db48539030db9de33a8681
出典データセット
uspto-grants-1981_07
特許番号
US04277610

反応ノート

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