HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 263321Erstellt: 25. Oktober 2026
Tetrahydrofuran → trans-5,6,7,8-Tetrahydro-1,6,7-naphthalenetriol
https://huagongshe.com/reaction/263321
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Perchloric Acid | HCID 24247 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 1a,2,7,7a-Tetrahydronaphtho[2,3-b]oxiren-3-ol | HCID 12445737 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | trans-5,6,7,8-Tetrahydro-1,6,7-naphthalenetriol | HCID 12445740 | — |
Reaktionsschritte
A solution of 8.0 g. (0.048 mole) of 5,6,7,8-tetrahydro-6,7-epoxy-1-naphthol in 100 ml. of tetrahydrofuran is cooled to 0° and 20 ml. of water and 0.5 ml. of 70% perchloric acid are added. After 4 hr., a further 1.5 ml. of acid is added and the solution stirred for 16 hr. at ambient temperature and diluted with 100 ml. each of ether, 10% sodium bicarbonate and saturated salt solution. The aqueous layer is separated and washed with 150 ml. of 1:1 ether-tetrahydrofuran. The organic phase is washed with saturated salt solution, dried and evaporated to give an oil which solidifies on trituration with chloroform. Recrystallization gives in two crops, 4.85 g. of solid which is recrystallized from ethyl acetate to give 3.84 g. m.p. 179.5°-181.5°. Two further recrystallizations of a small sample give the analytical specimen, m.p. 183°-184°.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04156789 |
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| Quelldatensatz | uspto-grants-1979_05 |
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| ORD ID | ord-707bbee21326442cb2c82c2e0412f233 |
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| Quellennotiz | uspto-grants-1979_05 |
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