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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1581076Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1581076

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 q. (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 hrs., 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
PatentnummerUS03935267
Quelldatensatzuspto-grants-1976_01
ORD IDord-0a40a0a2a7304e78b3254f12a84284c0
Quellennotizuspto-grants-1976_01