p-Toluenesulfonic acid → HCID 86735829, Verbindung

HRID 866367Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 866367
[S:1]1[CH2:5][CH2:4][S:3][CH:2]1[CH2:6][CH2:7][CH:8]1[CH:19](/[CH:20]=[CH:21]/[CH:22]([OH:28])[CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[CH2:18][CH2:17][C:9]21[O:14][CH2:13][C:12]([CH3:16])([CH3:15])[CH2:11][O:10]2.C1(C)C=CC(S(O)(=O)=O)=CC=1.[O:40]1[CH:45]=[CH:44][CH2:43][CH2:42][CH2:41]1.C([O-])([O-])=O.[Na+].[Na+]>CCOCC>[S:1]1[CH2:5][CH2:4][S:3][CH:2]1[CH2:6][CH2:7][CH:8]1[CH:19](/[CH:20]=[CH:21]/[CH:22]([OH:28])[CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])[CH2:18][CH2:17][C:9]21[O:14][CH2:13][C:12]([CH3:16])([CH3:15])[CH2:11][O:10]2.[O:40]1[CH2:41][CH2:42][CH2:43][CH2:44][CH:45]1[O:14][CH:9]1[CH2:17][CH2:18][CH2:19][CH2:20][O:10]1

Komponenten

6

Versuchsvorschrift

1.1 g (2.5 mmoles of 1-[7-[(1,3-dithia-2-cyclopentyl)-ethyl]-3,3-dimethyl-1,5-dioxaspiro[5,4]-dec-8-yl]-trans-1-octene-3-ol were dissolved in 20 ml of absolute ether, 20 mg of p-toluenesulfonic acid were added, 1.2 ml (13 mmoles) of dihydropyrane in 10 ml of absolute ether were added dropwise and the whole was stirred for 4 hours at room temperature. 0.2 ml of dihydropyrane was again added. The reaction mixture was allowed to stand overnight and was then stirred for 30 minutes with 0.5 g of solid Na2CO3. The suspension was filtered, the filtrate was concentrated under reduced pressure and the oil that had formed was eluted with cyclohexane-ethyl acetate (9:1) over a silica gel column.

Aufarbeitung

  1. waitto stand overnight
  2. filtrationThe suspension was filtered
  3. concentrationthe filtrate was concentrated under reduced pressure
  4. customthe oil that had formed
  5. washwas eluted with cyclohexane-ethyl acetate (9:1) over a silica gel column

Quellen und Nachweise

ORD-Eintrag
ord-b5ed18aee1354a4a91a8ea2251114516
Quelldatensatz
uspto-grants-1978_07
Patentnummer
US04098815

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