Cyanic acid → Tetrahydropyranyl ether

HRID 64921

Reaktionsgleichung

Reaktionsgleichung von HRID 64921
[C:1]([OH:3])#N.[O:4]1[CH:9]=[CH:8][CH2:7][CH2:6][CH2:5]1.[C:10]1(C)C=C[C:13](S(O)(=O)=O)=[CH:12][CH:11]=1.CC[O:23]CC>C(Cl)Cl>[O:4]1[CH2:5][CH2:6][CH2:7][CH2:8][CH:9]1[O:23][CH:13]1[CH2:12][CH2:11][CH2:10][CH2:1][O:3]1

Komponenten

6

Edukt 4

HCID 540Cyanic acidHCID 3283Diethyl EtherHCID 6101p-Toluenesulfonic acidHCID 80803,4-dihydro-2H-pyran

Produkt 1

HCID 263182Tetrahydropyranyl ether

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

A solution of 1.23 g of Part F cyano-alcohol (7.36 mmole) in 20 ml of dry methylene chloride was treated with 800 ml of dihydropyran (8.89 mmole) and catalytic amount of p-toluene sulfonic acid at 0°-5° C. After 4 hours, the reaction mixture was diluted with ether and washed with aqueous sodium bicarbonate solution. The aqueous layer was reextracted twice with ether. The combined organic extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The crude residue was chromatographed on a silica gel column and eluted with 2 ethyl acetate in hexane to obtain 1.61 g of title tetrahydropyranyl ether.

Aufarbeitung

  1. washwashed with aqueous sodium bicarbonate solution
  2. extractionThe combined organic extract
  3. dry with materialwas dried over anhydrous magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe crude residue was chromatographed on a silica gel column
  6. washeluted with 2 ethyl acetate in hexane

Quellen und Nachweise

ORD-Eintrag
ord-fb020a548ac8493380d7e8595f454fac
Quelldatensatz
uspto-grants-1986_09
Patentnummer
US04611005

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