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

HRID 1581076Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1581076
[O:1]1[CH:11]2[CH:2]1[CH2:3][C:4]1[CH:5]=[CH:6][CH:7]=[C:8]([OH:12])[C:9]=1[CH2:10]2.[O:13]1CCCC1.Cl(O)(=O)(=O)=O.C(=O)(O)[O-].[Na+]>C(Cl)(Cl)Cl.CCOCC.O>[C:8]1([OH:12])[C:9]2[CH2:10][C@@H:11]([OH:1])[C@H:2]([OH:13])[CH2:3][C:4]=2[CH:5]=[CH:6][CH:7]=1

Komponenten

8

Edukt 4

HCID 8028TetrahydrofuranHCID 24247Perchloric AcidHCID 516892Sodium BicarbonateHCID 124457371a,2,7,7a-Tetrahydronaphtho[2,3-b]oxiren-3-ol

Produkt 1

HCID 12445740trans-5,6,7,8-Tetrahydro-1,6,7-naphthalenetriol

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 962WaterLösungsmittelHCID 3283Diethyl EtherLösungsmittelHCID 6212ChloroformLösungsmittel

Versuchsvorschrift

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°.

Aufarbeitung

  1. additionof acid is added
  2. additionat ambient temperature and diluted with 100 ml
  3. customThe aqueous layer is separated
  4. washwashed with 150 ml
  5. washThe organic phase is washed with saturated salt solution
  6. customdried
  7. customevaporated
  8. customto give an oil which
  9. customRecrystallization
  10. customgives in two crops, 4.85 g
  11. customof solid which is recrystallized from ethyl acetate
  12. customto give 3.84 g
  13. customTwo further recrystallizations of a small sample
  14. customgive the analytical specimen, m.p. 183°-184°

Quellen und Nachweise

ORD-Eintrag
ord-0a40a0a2a7304e78b3254f12a84284c0
Quelldatensatz
uspto-grants-1976_01
Patentnummer
US03935267

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