関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | Trimethylolpropane | HCID 6510 | — |
| 反応物 | 3-Hydroxy-2,2-dimethylpropionaldehyde | HCID 11699 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 溶媒 | Cyclohexane | HCID 8078 | — |
| 生成物 | 2,2-Dimethyl-3-hydroxypropanal trimethylolpropane | HCID 86740262 | — |
反応手順
250 parts of 2,2-dimethyl-3-hydroxypropanal, 328 parts of trimethylolpropane, 16.4 parts of p-toluenesulfonic acid, 520 parts of benzene and 130 parts of cyclohexane were charged in a 2-1 reactor provided with a stirrer, thermostat, thermometer, condenser and separator. The mixture was heated. Water formed was distilled together with the solvent and condensed. Water alone was taken out of the system by means of the separator and the solvent was returned into the reactor. When 44 parts of water was formed, the reaction system was cooled. The reaction temperature was 70° to 85° C. The reaction mixture was dissolved in 2400 parts of benzene and 600 parts of cyclohexane and washed with 500 parts of a 20% aqueous common salt solution three times. The solvents were distilled off under reduced pressure to obtain 2,2-dimethyl-3-hydroxypropanal/trimethylolpropane condensate. The condensate was a white solid having a hydroxyl value of 515.1 and a melting point of 119° to 120.8° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04536588 |
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| 出典データセット | uspto-grants-1985_08 |
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| ORD ID | ord-e7e30b1a0218464087177eb92ad41389 |
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| 出典メモ | uspto-grants-1985_08 |
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