Acetic Acid → HCID 21853908、化合物

HRID 2072314ノート

反応式

HRID 2072314 の反応式
[C:1]([O:4][C:5]1[C:14]2[C:13]3[CH2:15][CH:16]([CH3:19])[CH2:17][CH2:18][C:12]=3[C:11]([CH3:21])([CH3:20])[O:10][C:9]=2[CH:8]=[C:7]([CH:22]([CH3:30])[CH:23]([CH3:29])[CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[CH:6]=1)(=[O:3])[CH3:2].C(Cl)(Cl)Cl.C(O)(=[O:37])C>>[C:1]([O:4][C:5]1[C:14]2[C:13]3[CH2:15][CH:16]([CH3:19])[CH2:17][C:18](=[O:37])[C:12]=3[C:11]([CH3:20])([CH3:21])[O:10][C:9]=2[CH:8]=[C:7]([CH:22]([CH3:30])[CH:23]([CH3:29])[CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])[CH:6]=1)(=[O:3])[CH3:2]

参加物

4

実験手順

To a stirring mixture of 1-acetoxy-3-(1,2-dimethylheptyl)-7,8,9,10-tetrahydro-6,6,9-trimethyl-6H-dibenzo[ b,d]pyran (5.21 g., 12.6 mmole) in 35 ml. of 50% acetic acid and 10 ml. of chloroform under a nitrogen atmosphere, was added dropwise a solution of ceric ammonium nitrate (27.63 g., 50.4 mmole) in 70 ml. of 50% acetic acid. After the addition was complete, the reaction mixture was stirred over a steam bath. After 3 hours the mixture was poured onto ice with stirring. It was extracted into ether and the organic solvents were removed under reduced pressure. The residue was again taken up in ether, washed to neutrality with 5% NaHCO3, washed with water and dried over Na2SO4. Evaporation of the solvents in vacuo left 8.34 g. (23%) of crude product whose tlc showed a blue fluorescent spot (silica gel, Rf 0.66, 1:1 EtOAc/hexane).

後処理

  1. additionAfter the addition
  2. additionAfter 3 hours the mixture was poured onto ice
  3. stirringwith stirring
  4. extractionIt was extracted into ether
  5. customthe organic solvents were removed under reduced pressure
  6. washwashed
  7. washwashed with water
  8. dry with materialdried over Na2SO4
  9. customEvaporation of the solvents in vacuo
  10. waitleft 8.34 g

出典と根拠

ORDレコード
ord-bd2d4c5bb7624942b5b47c79337ce369
出典データセット
uspto-grants-1977_09
特許番号
US04051152

反応ノート

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