Dichloromethane → 1-(2,2,4-Trimethyl-3-cyclohexen-1-yl)ethan-1-one

HRID 42728

反応式

HRID 42728 の反応式
[CH3:1]C(=O)C=C.[CH2:6]1[CH2:10][O:9][CH2:8][CH2:7]1.[CH3:11][C:12]([CH:14]=[C:15](C)[CH3:16])=[CH2:13].ClCCl>[Cl-].[Al+3].[Cl-].[Cl-].O>[CH3:11][C:12]1([CH3:13])[CH:14]=[C:15]([CH3:16])[CH2:10][CH2:6][CH:7]1[C:8](=[O:9])[CH3:1]

参加物

7

反応物 4

HCID 6344DichloromethaneHCID 6570Methyl vinyl ketone2 回HCID 8028TetrahydrofuranHCID 660802,4-Dimethylpenta-1,3-diene

生成物 1

HCID 30169881-(2,2,4-Trimethyl-3-cyclohexen-1-yl)ethan-1-one収率 971.6%

試薬・触媒・溶媒 2

HCID 6451240Aluminum(III) Chloride触媒HCID 962Water溶媒

反応条件

温度
5 °C

実験手順

In a 500 ml sulfonation flask with cooling funnel, dropping funnel and mechanical stirring under air (*) at 5° C. was added but-3-en-2-one (43 ml; 0.52 mol) then THF (4.2 ml; 52 mmol) followed by a careful portionwise addition of aluminum chloride (3.5 g; 26 mmol). White fumes and increase of temperature to 20° C. were observed. The mixture turned red. The temperature was decreased to 15° C. and 2,4-dimethyl-1,3-pentadiene (68 ml; 0.52 mol) was added dropwise (90 min). Exothermic reaction was observed. The reaction mixture was stirred for 8 hours at 25° C. and for 10 hours at 45° C. As the diene was still detected but-3-en-2-one was added dropwise (22 ml; 0.26 mol) (10 min) and the mixture was stirred for additional 48 hours at 25° C. Dichloromethane (200 ml) was added to the mixture which was stirred for 5 min and filtered over celite. The red solution obtained was poured into cold water (1 l) and extracted with dichloromethane (4×300 ml). Combined organic layers were washed with brine (500 ml) and water (500 ml), dried over sodium sulfate and filtered over silica. The solvent was removed in vacuo to afford 84 g (97% of theory) of 1-(2,2,4-trimethyl-cyclohex-3-enyl)-ethanone as a clear red oil.

後処理

  1. temperatureIn a 500 ml sulfonation flask with cooling funnel
  2. temperatureWhite fumes and increase of temperature to 20° C.
  3. customwas decreased to 15° C.
  4. customExothermic reaction
  5. stirringThe reaction mixture was stirred for 8 hours at 25° C. and for 10 hours at 45° C
  6. additionwas added dropwise (22 ml; 0.26 mol) (10 min)
  7. stirringthe mixture was stirred for additional 48 hours at 25° C
  8. stirringwas stirred for 5 min
  9. filtrationfiltered over celite
  10. customThe red solution obtained
  11. extractionextracted with dichloromethane (4×300 ml)
  12. washCombined organic layers were washed with brine (500 ml) and water (500 ml)
  13. dry with materialdried over sodium sulfate
  14. filtrationfiltered over silica
  15. customThe solvent was removed in vacuo

出典と根拠

ORDレコード
ord-e7df1f8a82a34de188cef0a297aaf5de
出典データセット
uspto-grants-2013_09
特許番号
US08536215B2

関連ノート

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