tert-Butyl hydroperoxide → (trans)-3-(7-Phenyl-1,2-heptadiene-4,6-diynyl)oxiranemethanol

HRID 1906976

反応式

HRID 1906976 の反応式
[C:1]1([C:7]#[C:8][C:9]#[C:10][CH:11]=[C:12]=[CH:13][CH:14]=[CH:15][CH2:16][OH:17])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C([O:22]O)(C)(C)C>C1C=CC=CC=1.C/C(/O)=C\C(C)=O.C/C(/O)=C\C(C)=O.O=[V]>[C:1]1([C:7]#[C:8][C:9]#[C:10][CH:11]=[C:12]=[CH:13][C@@H:14]2[O:22][C@H:15]2[CH2:16][OH:17])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

参加物

5

反応物 2

HCID 6410tert-Butyl hydroperoxideHCID 5394307710-Phenyl-7,9-decadiyne-2,4,5-trien-1-ol

生成物 1

HCID 86740795(trans)-3-(7-Phenyl-1,2-heptadiene-4,6-diynyl)oxiranemethanol

試薬・触媒・溶媒 2

HCID 16217092Bis(2,4-pentanedionato)vanadium(IV) Oxide触媒HCID 241Benzene溶媒2 回

実験手順

To a stirred solution of 20 mg (0.090 mmole) of 10-phenyl-7,9-decadiyne-2,4,5-trien-1-ol in 4 ml of benzene was added 2 mg of vanadyl acetylacetonate and 50 μl (0.26 mmole) of a 5.43M solution of t-butyl hydroperoxide in benzene. The mixture was stirred for two hours. The mixture was concentrated and the residue was purified via flash chromatography to afford 7 mg of the title compound as an approximately 1:1 mixture of diastereomers.

後処理

  1. concentrationThe mixture was concentrated
  2. customthe residue was purified via flash chromatography

出典と根拠

ORDレコード
ord-fa7e7b7cf5b94c54b0702566d67516c3
出典データセット
uspto-grants-1987_03
特許番号
US04654426

関連ノート

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