Carbon Dioxide → Dihexyl carbonate

HRID 2115592

反応式

HRID 2115592 の反応式
[CH2:1]([OH:7])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[C:8](=[O:10])=[O:9]>>[C:8](=[O:10])([O:9][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH3:6])[O:7][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH3:6]

参加物

3

反応条件

温度
30 °C

実験手順

Into the above-mentioned 200-ml autoclave containing the reaction mixture (containing an organometal compound having a hexyloxy group) was charged 61.5 g (602 mmol) of hexanol (manufactured and sold by Aldrich, U.S.A.; a dehydrated grade), and the autoclave was sealed. Then, from a carbon dioxide gas bomb, carbon dioxide gas, the pressure of which was lowered to 5 MPa by means of a pressure regulator connected to the carbon dioxide gas bomb, was introduced into the autoclave. Stirring of the contents of the autoclave was started. 10 Minutes after the start of the stirring, the valve of the carbon dioxide gas bomb was closed. Then, the internal temperature of the autoclave was elevated to 180° C. while stirring. In this instant, the internal pressure of the autoclave was about 7.5 MPa. Then, a reaction was performed for 6 hours while maintaining the internal pressure of the autoclave at about 7.5 MPa. Thereafter, the inside of the autoclave was cooled to about 30° C. and the internal pressure of the autoclave was returned to atmospheric pressure by gently purging the carbon dioxide gas, and there was obtained a transparent reaction mixture. In the reaction mixture, dihexyl carbonate was obtained in a yield of about 14%.

後処理

  1. additionInto the above-mentioned 200-ml autoclave containing the reaction mixture (
  2. additioncontaining an organometal compound
  3. customa dehydrated grade), and the autoclave was sealed
  4. additionwas introduced into the autoclave
  5. customwas elevated to 180° C.
  6. stirringwhile stirring
  7. temperaturewhile maintaining the internal pressure of the autoclave at about 7.5 MPa
  8. customby gently purging the carbon dioxide gas
  9. customthere was obtained a transparent reaction mixture

出典と根拠

ORDレコード
ord-82f91df692234f96b02e671530511088
出典データセット
uspto-grants-2008_10
特許番号
US07435842B2

関連ノート

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