反応式
[CH2:1]([OH:8])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][OH:7].[C:9](=[O:14])([O:12][CH3:13])[O:10][CH3:11].C[O-].C([Sn+2]CCCC)CCC.C[O-]>>[CH2:1]([OH:8])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][OH:7].[CH3:11][O:10][C:9](=[O:14])[O:12][CH3:13]参加物
4
反応条件
- 温度
- 220 °C
実験手順
391 g (3.32 moles) of 1,6-hexanediol, 5976 g (66.4 moles) of dimethyl carbonate and 0.2 g (0.00067 mole) of dibutyltin methoxide were charged in an autoclave. The mixture was heated at 220° C. for 3 hours to advance a reaction. After completion of the reaction, the dimethyl carbonate was removed by evaporation under reduced pressure to obtain a 1,6-hexanediol bismethylcarbonate. The yield of 1,6-hexanediol bismethylcarbonate was 98.0%. A 1,5-pentanediol bismethylcarbonate was also obtained in substantially the same manner as mentioned above except that 1,5-pentane diol was used instead of 1,6-hexane diol.
後処理
- customa reaction
- customAfter completion of the reaction
- customthe dimethyl carbonate was removed by evaporation under reduced pressure
出典と根拠
- ORDレコード
- ord-ef45616f6a7c4a91900eaf9db2c126b2
- 出典データセット
- uspto-grants-1989_08
- 特許番号
- US04855377
関連ノート
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