Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 12407526 | HCID 12407526 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 23499685 | HCID 23499685 | 82.7% |
Reaction Steps
Into a 100 ml four-necked flask were charged 29.96 g of 1,4-bis[1-(4-hydroxy-3-methylphenyl)-1-methylethyl]benzene["Bis-OC-P" manufactured by Honshu Kagaku Co., Ltd.], 4.48 g of sodium hydroxide and 44.8 g of water. While stirring at 50° C., 25.97 g of 37% formaldehyde was added dropwise thereto over 1 hour, and the reaction was conducted for 1 more hour. After completion of the reaction, 11 g of 90% aqueous acetic acid solution was added for neutralization and then the mixture was cooled to 25° C. Thereafter, 100 g of ethyl acetate and20 g of toluene were added thereto and a phase separation was carried out. The separated solution was concentrated and 100 g of hexane was added to the concentrated mass and it was cooled to 25° C. The resulting mixture was filtered, and the filtered product was rinsed with 100 g of hexane and dried a whole day and night at 45° C. under reduced pressure to obtain 28.75 g of 1,4-bis[1-(4-hydroxy-3-hydroxymethyl-5-methylphenyl)-1-methylethyl]benzene
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05866724 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-6dbd6a360d6147258a07847131cac87d |
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| Source note | uspto-grants-1999_02 |
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