Tetrahydrofuran → CID 3084433

HRID 1758115

反応式

HRID 1758115 の反応式
[B-](F)(F)(F)F.[K+].[O:7]1[CH2:11][CH2:10][CH2:9][CH2:8]1>S(=O)(=O)(O)O>[CH3:8][CH2:9][CH2:10][CH2:11][O:7][C@H:10]([CH2:11][OH:7])[CH2:9][CH3:8]

参加物

4

反応条件

温度
10 °C

実験手順

In the same reaction apparatus as in Example 1, a solution prepared by dissolving 0.82 g of potassium borofluoride in 105 g of 25% fuming sulfuric acid was drowpise added to 500 g of tetrahydrofuran at -10° C. over a period of 40 minutes, and thereafter the mixture was subjected to reaction at -10° C. for one hour. The tetrahydrofuran conversion at the end of this reaction was 38%. Then, the reaction mixture was heated to 10° C. and further subjected to reaction for 2 hours. The conversion at the end of this reaction was 60%. Neither solidification nor coloration of the reaction system was observed in the entire course of the reaction. The polymerization product was then treated in the same manner as in Example 1 to obtain colorless PTMG. Its analytical results and the catalytic efficiency α were as shown in Table 1.

後処理

  1. customIn the same reaction apparatus as in Example 1, a solution prepared
  2. customthe mixture was subjected to reaction at -10° C. for one hour
  3. customfurther subjected to reaction for 2 hours
  4. customNeither solidification nor coloration of the reaction system was observed in the entire course of the reaction
  5. additionThe polymerization product was then treated in the same manner as in Example 1

出典と根拠

ORDレコード
ord-9ea3de2b5b874751a319a4a5a95402fb
出典データセット
uspto-grants-1983_02
特許番号
US04371713

関連ノート

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