Benzoyl Peroxide → 7-Thia-tetradecan-5-ene-1-ol
Reaktionsgleichung
[CH2:1]([SH:8])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7].[CH2:9]([OH:15])[CH2:10][CH2:11][CH2:12][C:13]#[CH:14].C(OOC(=O)C1C=CC=CC=1)(=O)C1C=CC=CC=1.C(=O)(O)[O-].[Na+]>CCCCCCC>[CH2:9]([OH:15])[CH2:10][CH2:11][CH2:12][CH:13]=[CH:14][S:8][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7]Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To 1.332 gr (10 mmol) of n-heptyl mercaptan and 981 mg (10 mmol) of 5-hexyn-1-ol dissolved in 25 ml of heptane under an argon atmosphere was added a few crystals of dibenzoyl peroxide. The reaction was stirred magnetically and heated to reflux for 18 hours. It was then cooled and poured into 25 ml of 10% sodium bicarbonate and extracted with 3×25 ml of ethyl acetate. The organic phases were combined and dried over sodium sulfate, filtered, and evaporated to yield a yellow oil. The oil was chromatographed on eight silica gel type GF preparative plates, using hexane-ethyl acetate (4:1) as developing solvent. Following removal of the band corresponding to product from the plates, the product was extracted from the silica with methanol, 684 mg (30% yield) of pure 7-thia-tetradecan-5-ene-1-ol was obtained as a pale yellow oil.
Aufarbeitung
- temperatureheated
- temperatureto reflux for 18 hours
- temperatureIt was then cooled
- extractionextracted with 3×25 ml of ethyl acetate
- dry with materialdried over sodium sulfate
- filtrationfiltered
- customevaporated
- customto yield a yellow oil
- customThe oil was chromatographed on eight silica gel type GF preparative plates
- customremoval of the band corresponding to product from the plates
- extractionthe product was extracted from the silica with methanol
Quellen und Nachweise
- ORD-Eintrag
- ord-4d4938ca67734d77ac015dae80732845
- Quelldatensatz
- uspto-grants-1992_05
- Patentnummer
- US05116726
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