Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Hexane-1,6-dione, 1,6-bis(2,4-dihydroxyphenyl)- | HCID 283375 | — |
| Catalyst | Tetramethylammonium chloride | HCID 6379 | — |
| Product | HCID 20213775 | HCID 20213775 | — |
Reaction Steps
18.16 g (0.055 mole) of 1,4-bis-(2',4'-dihydroxybenzoyl)-butane, 86.84 g (0.938 mole) of epichlorohydrin and 0.97 g of 50% aqueous tetramethylammonium chloride solution are initially placed in a 350 ml sulfonation flask equipped with a stirrer, a thermometer, a condenser, a dropping funnel and a water separator, and are heated at 105°-110° C. After a reaction time of 4 hours the reaction mixture is cooled to 60° C.; 20.21 g (0.253 mole) of 50% aqueous sodium hydroxide solution are then added with simultaneous removal of water from the system. The resulting suspension is treated with water, and the organic phase is washed with water, dried over sodium sulphate and concentrated. This gives 28.62 g (93.84% of theory) of a red, viscous resin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04649181 |
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| Source dataset | uspto-grants-1987_03 |
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| ORD ID | ord-9008c956e24f4443874f47cd15f0a104 |
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| Source note | uspto-grants-1987_03 |
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