Sulfuric Acid → HCID 21906966、化合物

HRID 1246962

反応式

HRID 1246962 の反応式
[C:1]1([C:7]2([C:11]([OH:13])=O)[CH2:10][CH2:9][CH2:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.OS(O)(=O)=O.[N+:19]([O-])([O-:21])=[O:20].[K+].[BH4-].[Na+].B(F)(F)F.CCOCC>C(O)(=O)C>[N+:19]([C:4]1[CH:5]=[CH:6][C:1]([C:7]2([CH2:11][OH:13])[CH2:10][CH2:9][CH2:8]2)=[CH:2][CH:3]=1)([O-:21])=[O:20]

参加物

7

反応条件

温度
0 °C

実験手順

A mixture of 1-phenylcyclobutanecarboxylic acid (10) and acetic acid (20 ml) and H2SO4 (20 ml) and KNO3 (1.1 eq) was stirred at 0° C. for 20 min. The mixture was warmed to RT and stirred overnight. The mixture was poured on ice and stirred until all ice melted. The precipitate was filtered and used for next step without further purification. The above product (5 g) was dissolved into THF and stirred at 0° C., NaBH4 (3 eq) was added slowly to the reaction followed by slowly addition of BF3.Et2O (3 eq). The reaction was stirred at RT overnight and quenched with 1 N NaOH slowly until bubble ceased. The solution was extracted with EtOAc and washed with H2O followed by brine, dried over Na2SO4 and evaporated. The residue was purified by column chromatography to give [(4-nitrophenyl)cyclobutyl]methane-1-ol as an oil.

後処理

  1. temperatureThe mixture was warmed to RT
  2. stirringstirred overnight
  3. additionThe mixture was poured on ice
  4. stirringstirred until all ice
  5. filtrationThe precipitate was filtered
  6. customused for next step without further purification
  7. dissolutionThe above product (5 g) was dissolved into THF
  8. stirringstirred at 0° C.
  9. stirringThe reaction was stirred at RT overnight
  10. customquenched with 1 N NaOH slowly
  11. customuntil bubble
  12. extractionThe solution was extracted with EtOAc
  13. washwashed with H2O
  14. dry with materialdried over Na2SO4
  15. customevaporated
  16. customThe residue was purified by column chromatography

出典と根拠

ORDレコード
ord-fb4db718258847b8ab10cea653cd66ad
出典データセット
uspto-grants-2006_10
特許番号
US07129252B2

関連ノート

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