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Ethyl geranate

The 5 (or 6)HF Et3N system reacts with a variety of branched alkenes to give tertiary alkyl fluorides. Hydrofluorination of dienes proceeds at the more reactive C = C bond selectively. Thus, ethyl geranate (1) and ethyl nerolate (2) react with 5HF EtaN at the noncon-... [Pg.107]

Ethyl geranate (50) has been synthesized highly stereoselectively (Scheme 5).136 An alternative route to the ester (51) by y-alkylation of 2-butynoic acid has been... [Pg.17]

Figure 5.6 GC-MS analyses of a White Muscat wine by SPE wine aroma enrichment using a C18 pre-packed cartridge (a) and a XAD-2 hand-made cartridge (b) performed in the same analytical conditions (Versini et al., 1995). 1. isoamyl acetate, 2. ethyl hexanoate, 3. 1-hexanol, 4. linalool, 5. ho-trienol, 6. ethyl decanoate, 7. diethyl succinate, 8. a-terpineol, 9. trans pyran linalooloxide, 10. hexanoic acid, 11. Ho-diendiol (I), 12. octanoic acid, 13. Ho-diendiol (II), 14. diethyl 2-hydroxyglutarate, 15. hydroxycitronellol, 16. decanoic acid, 17. trans 8-hydroxylinalool, 18. cis 8-hydroxylinalool, 19. trans geranic acid, 20. 4-vinylphenol... Figure 5.6 GC-MS analyses of a White Muscat wine by SPE wine aroma enrichment using a C18 pre-packed cartridge (a) and a XAD-2 hand-made cartridge (b) performed in the same analytical conditions (Versini et al., 1995). 1. isoamyl acetate, 2. ethyl hexanoate, 3. 1-hexanol, 4. linalool, 5. ho-trienol, 6. ethyl decanoate, 7. diethyl succinate, 8. a-terpineol, 9. trans pyran linalooloxide, 10. hexanoic acid, 11. Ho-diendiol (I), 12. octanoic acid, 13. Ho-diendiol (II), 14. diethyl 2-hydroxyglutarate, 15. hydroxycitronellol, 16. decanoic acid, 17. trans 8-hydroxylinalool, 18. cis 8-hydroxylinalool, 19. trans geranic acid, 20. 4-vinylphenol...
Thermolysis of the sulfone 58 gave 58% of a mixture of geraniol (25) and nerol (27) ethyl ethers. Starting from senecioic acid (59), Katzenellenbogen has continued studies of the addition of prenyl halides (15, R = halogen) to the dianion in presence of copper. Copper ion also influenced the addition of prenyl bromide (15, R = Br) to the anion of the V-methylamide of 59, its presence transforming a yield of 98% of the a-addition product to 83% of the y-product, geranic acid V-methylamide [as a mixture of (Z)- and ( )-isomers]. ... [Pg.288]

Ethyl geranate has been prepared stereoselectively under phase-transfer conditions by prenylation of ethyl -3-methyl-4-benzenesulphonylbut-2-enoate and desulphurization. Biomimetic synthesis of (39) from dimethylallyl acetate and isopentenyl acetate (1 3) catalysed by LiC104-Ac0H has been examined the corresponding alcohol (40) is obtained efficiently from isopentenyl acetate by... [Pg.30]

A total synthesis of ethyl geranate (28) makes use of the addition of ethyl 4-bromo-3-methylbut-2-enoate (29) to the nickel carbonyl complex (30) of prenyl bromide. Geranyl acetate and the ethyl ether were made in a similar way. ... [Pg.15]


See other pages where Ethyl geranate is mentioned: [Pg.269]    [Pg.58]    [Pg.293]    [Pg.1050]    [Pg.22]    [Pg.33]    [Pg.35]    [Pg.52]    [Pg.5322]    [Pg.398]    [Pg.164]    [Pg.146]   
See also in sourсe #XX -- [ Pg.293 ]




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