(4R)-5,5-Dimethyl-2-phenyl-1,3-dioxan-4-carbaldehyde → (4S)-5,5-Dimethyl-2-phenyl-4-vinyl-1,3-dioxane
Reaktionsgleichung
[Li][CH2:2]CCC.[CH3:6][C:7]1([CH3:21])[CH2:12][O:11][CH:10]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[O:9][C@H:8]1[CH:19]=O>[Br-].C[P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.O1CCCC1>[CH3:21][C:7]1([CH3:6])[CH2:12][O:11][CH:10]([C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)[O:9][C@H:8]1[CH:19]=[CH2:2]Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
Following the general procedure for methylenation via Wittig-olefination of Description 8, a phosphorous ylide generated from 17.86 g (50.0 mmol) of methyltriphenylphosphonium bromide and 31.0 mmol of n-BuLi in 125 mL of anhydrous tetrahydrofuran (THF), was reacted with 5.5 g (25.0 mmol) of (4R)-5,5-dimethyl-2-phenyl-1,3-dioxan-4-carbaldehyde (7b). Aqueous work-up followed by purification using column chromatography with mixtures of methyl tert-butyl ether (MTBE) and hexanes (Hxn) as eluent (MTBE/Hxn=9:1→MTBE/Hxn=6:1) provided 4.67 g (86% yield) of the title compound (7c) as a yellowish liquid. Rf=0.66 (MTBE/Hxn=1:6). 1H NMR (400 MHz, CHCl3): δ=0.82 (s, 3H), 1.16 (s, 3H), 3.67 (d, J=10.8 Hz, 1H), 3.78 (d, J=10.8 Hz, 1H), 4.05 (d, J=6.0 Hz, 1H), 5.24-528 (m, 1H), 5.31-5.37 (m, 1H), 5.55 (s, 1H), 5.87 (ddd, J=17.6, 10.4, 6.0 Hz, 1H), 7.30-7.40 (m, 3H), 7.52-7.55 (m, 2H) ppm. MS (ESI) m/z: 219.1 (M+H)+. The analytical data was consistent with that given in the literature (Ito, et al., Synthesis 1993, 137-140).
Aufarbeitung
- customAqueous work-up followed by purification
Quellen und Nachweise
- ORD-Eintrag
- ord-73eb4bb978aa48f6a32128434cd104ef
- Quelldatensatz
- uspto-grants-2012_05
- Patentnummer
- US08168617B2
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