Mycophenolic acid glucuronide → 2,6-Bisformyl bicyclo[2.2.1]heptane

HRID 587809ノート

反応式

HRID 587809 の反応式
[C]=O.[H][H].[CH3:5][C:6]1[C:11]2CO[C:14](=[O:15])[C:10]=2[C:9](O[C@@H]2O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]2O)=[C:8]([CH2:29]/C=C(/CCC(O)=O)\C)[C:7]=1OC.C(C1CC2CC1CC2C=O)=[O:41]>>[CH:14]([CH:10]1[CH2:9][CH:8]2[CH2:29][CH:11]1[CH:6]([CH:5]=[O:41])[CH2:7]2)=[O:15]

参加物

5

反応条件

温度
100 °C

実験手順

Next, the inside of the autoclave was sufficiently substituted by nitrogen, and then sufficiently substituted by a gas mixture having a volume ratio of carbon monoxide to hydrogen of 50/50. The same gas was injected until a pressure in the autoclave reached 0.6 MPaG, and the adjustment liquid was heated to 100° C. under stirring, thereby initiating a hydroformylation reaction. Since the pressure in the autoclave decreased with proceeds of the reaction, the gas mixture was continuously supplied so that the pressure was maintained at 0.6 MPaG, the temperature was adjusted so as to be maintained at 100° C., and the hydroformylation reaction was carried out for 6 hours. After the completion of the reaction, the gas mixture in the system was purged using nitrogen, and 280.1 g of a reaction liquid including 2,5-bisformyl bicyclo[2.2.1]heptane and 2,6-bisformyl bicyclo[2.2.1]heptane was obtained. An analysis showed that the reaction liquid contained 266.1 g (1.76 mol) of the compounds.

後処理

  1. customa hydroformylation reaction
  2. customSince the pressure in the autoclave decreased with proceeds of the reaction
  3. temperatureto be maintained at 100° C.
  4. customthe hydroformylation reaction
  5. customAfter the completion of the reaction
  6. customthe gas mixture in the system was purged
  7. customnitrogen, and 280.1 g of a reaction liquid

出典と根拠

ORDレコード
ord-f34e81c568704f33a9176a4a0388a4ce
出典データセット
uspto-grants-2016_01
特許番号
US09227925B2

反応ノート

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