Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3-Dihydrofuran | HCID 70934 | — |
| Reactant | 3,4-Dihydroxystyrene | HCID 151398 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 19019067 | HCID 19019067 | — |
Reaction Steps
To 38.1 g (0.28 mol) of 3,4-dihydroxystyrene and 118 g (1.68 mol) of 2,3-dihydrofuran are added 5 drops of concentrated hydrochloric acid, whereupon an exothermic reaction ensues. The solution is stirred for 4 h at 50° C. and then poured on to a mixture of ice-water and diethyl ether. After two extractions with diethyl ether, the organic phase is washed three times at 0° C. with 1N NaOH and dried over Na2SO4. The solvent is removed by evaporation to leave a clear liquid which is purified by distillation in a bulb tube (155° C./0.02 torr) or by column chromatography (silica gel, hexane/ethyl acetate 4:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05324804 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-e92d55000f9145878b4ca5da59696b86 |
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| Source note | uspto-grants-1994_06 |
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