Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 53690090 | HCID 53690090 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57293049 | HCID 57293049 | — |
Reaction Steps
16.7 g of hydroquinone, 8.6 g of 85% KOH, 14 g of water and 200 ml of ethanol were added into a four-necked flask, and the reaction was carried out for 13 hours. After elevated in temperature to 50° C., the reaction was further carried out for 3 hours and 30 g of (2'-pentyloxypropyl) p-toluenesulfonate was added dropwise to the reaction mixture and at the temperature elevated to 70° C., the reaction was carried out for 1 hour and then for 3 hours by heating under reflux, and the mixture was left standing at room temperature for 22 hours. After 500 ml of water and a small amount of hydrochloric acid were added to the residue after evaporation of ethanol, the mixture was extracted with 500 ml of hexane. The product after washing twice with water was dried over Na2SO4, recrystallization was effected with hexane. Optical rotation [α]D28° =13.5°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05114613 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-4e831eda6124451bb5f742bd177060c5 |
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| Source note | uspto-grants-1992_05 |
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