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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTetrahydrofuranHCID 8028—
EduktPerchloric AcidHCID 24247—
EduktSodium BicarbonateHCID 516892—
Edukt1a,2,7,7a-Tetrahydronaphtho[2,3-b]oxiren-3-olHCID 12445737—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelChloroformHCID 6212—
Produkttrans-5,6,7,8-Tetrahydro-1,6,7-naphthalenetriolHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04156789
Quelldatensatzuspto-grants-1979_05
ORD IDord-707bbee21326442cb2c82c2e0412f233
Quellennotizuspto-grants-1979_05