Carbon Dioxide → 4-Vinyl-1-cyclohexene

HRID 224729

反応式

HRID 224729 の反応式
[Sn].N([O-])=O.[Na+].C(=O)=O.[CH2:9]=[CH:10][CH:11]=[CH2:12]>>[CH2:9]=[CH:10][CH:11]=[CH2:12].[CH:10]([CH:11]1[CH2:12][CH2:11][CH:10]=[CH:9][CH2:12]1)=[CH2:9]

参加物

6

反応物 4

HCID 280Carbon DioxideHCID 78451,3-ButadieneHCID 5352426Tin atomHCID 23668193Sodium Nitrite

生成物 2

HCID 74994-Vinyl-1-cyclohexeneHCID 78451,3-Butadiene

反応条件

温度
75 °C

実験手順

In a control run, the following reaction mixture was prepared in a Fisher-Porter aerosol compatibility bottle: 0.25 grams (1.5 mmol) of ferric chloride, 0.3 grams (2.5 mg-atom) of tin powder and 0.3 grams (4.5 mmol) of sodium nitrite. The bottle reactor was evacuated then flushed with nitrogen followed by the addition of 10 ml of THF. The mixture was cooled with dry ice and 18.3 grams (339 mmol) of 1,3-butadiene added. This reaction mixture was heated to 75° C. with stirring. During this time, the original dark green solution changed in color to an orange-brown color. After 5 hours, the reaction was terminated and the reaction mixture allowed to cool to room temperature and stand for 1 day. Pressure on the reactor was still at 25 psig indicating there had been little, if any, conversion of 1,3-butadiene to the dimer. The results of this run indicate that one does not obtain dimerization of 1,3-butadiene to 4-vinylcyclohexene if one attempts to form the iron nitrosyl halide simultaneously with the dimerization.

後処理

  1. customIn a control run, the following reaction mixture
  2. customwas prepared in a Fisher-Porter aerosol compatibility bottle
  3. customThe bottle reactor was evacuated
  4. customthen flushed with nitrogen
  5. additionfollowed by the addition of 10 ml of THF
  6. additionadded
  7. customthe reaction was terminated
  8. temperatureto cool to room temperature
  9. waitstand for 1 day
  10. customThe results of this run

出典と根拠

ORDレコード
ord-e4297e6d406d4d5eb80d2900b608f29c
出典データセット
uspto-grants-1980_11
特許番号
US04234454

関連ノート

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