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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1576692Erstellt: 26. Oktober 2026

Tetrahydrofuran → trans-5,6,7,8-Tetrahydro-1,6,7-naphthalenetriol

https://huagongshe.com/reaction/1576692

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
PatentnummerUS03982021
Quelldatensatzuspto-grants-1976_09
ORD IDord-f0496fda9bca4f0ea323f0a730f12c94
Quellennotizuspto-grants-1976_09