참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | p-Toluenesulfonic acid | HCID 6101 | — |
| 반응물 | Trimethylolpropane | HCID 6510 | — |
| 반응물 | 3-Hydroxy-2,2-dimethylpropionaldehyde | HCID 11699 | — |
| 용매 | Benzene | HCID 241 | — |
| 용매 | Cyclohexane | HCID 8078 | — |
| 생성물 | 2,2-Dimethyl-3-hydroxypropanal trimethylolpropane | HCID 86740262 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04536588 |
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| 출처 데이터셋 | uspto-grants-1985_08 |
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| ORD ID | ord-e7e30b1a0218464087177eb92ad41389 |
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| 출처 메모 | uspto-grants-1985_08 |
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