Réaction #1552080

Équation de réaction

Diiodomethane

diiodomethane

triethylaluminium

triethylaluminium

diiodomethane

triethylaluminium

3-chloroperbenzoic acid

1-(4-Isobutyl-6-methylcyclohex-3-enyl)ethanol

4b

1-(4-Isobutyl-6-methylcyclohex-3-enyl)ethanol

→

oil

Rendement 121.5%

1-(6-Isobutyl-4-methylbicyclo[4.1.0]heptan-3-yl)ethanol

Rendement 121.5%

Solvants

water

hexane

Conditions de réaction

Traitement

1. 1
   workup.ADDITIONwas added over 30 min while the temperature
2. 2
   Autrewas kept below 5°
3. 3
   Autreto return to room temperature
4. 4
   workup.STIRRINGAfter 2 h stirring
5. 5
   AutreThe phases were separated
6. 6
   Extractionthe aqueous one extracted twice with hexane
7. 7
   LavageThe combined organic layers were washed with water, twice with 2M HCl and again with water
8. 8
   Séchagedried (Na2SO4)
9. 9
   Autrethe solvent removed in vacuo
10. 10
    workup.DISSOLUTIONThe crude oil (5.7 g) was dissolved in methylene chloride (50 ml)
11. 11
    AutreThe mild exothermic effect was controlled with a cool water bath
12. 12
    Autrehad been completely consumed (30 min)
13. 13
    workup.ADDITION2M NaOH was added
14. 14
    workup.STIRRINGthe mixture stirred until it
15. 15
    AutreThe phases were separated
16. 16
    Extractionthe upper aqueous layer extracted twice with methylene chloride
17. 17
    LavageThe combined organic layers were washed twice with 2M NaOH and water
18. 18
    Séchagedried (MgSO4)
19. 19
    Autreevaporated in vacuo

Mode opératoire

Diiodomethane (9.6 g, 36 mmol) was added at room temperature, with stirring and under nitrogen, to a solution of 1-(4-Isobutyl-6-methylcyclohex-3-enyl)ethanol 4b (3.5 g, 18 mmol) in hexane (50 ml). After cooling to 5° C. triethylaluminium (1M, 36 ml, 36 mmol) was added over 30 min while the temperature was kept below 5°. The reaction was allowed to return to room temperature and stirred for 16 h, then another portion of diiodomethane (9.6 g, 36 mmol) and triethylaluminium (1M, 36 ml, 36 mmol) were added. After a further 15 h yet more diiodomethane (4.8 g, 18 mmol) and triethylaluminium (1M, 18 ml, 18 mmol) were added. After 2 h stirring, the reaction being still incomplete, the reaction mixture was poured slowly, onto a stirred mixture of ice and water. The phases were separated and the aqueous one extracted twice with hexane. The combined organic layers were washed with water, twice with 2M HCl and again with water, dried (Na2SO4) and the solvent removed in vacuo. The crude oil (5.7 g) was dissolved in methylene chloride (50 ml) and solid 3-chloroperbenzoic acid (ca. 77%, 1.5 g, 6.7 mmol) was added in four portions under nitrogen. The mild exothermic effect was controlled with a cool water bath. The reaction was stirred till the unreacted 4b had been completely consumed (30 min). 2M NaOH was added and the mixture stirred until it became white. The phases were separated and the upper aqueous layer extracted twice with methylene chloride. The combined organic layers were washed twice with 2M NaOH and water, dried (MgSO4) and evaporated in vacuo to give 4.6 g of oil. The crude oil was purified by flash chromatography (MTBE/hex. 3:2) and combination of pure fractions gave 5b as a 1:1.1:1.8 mixture of diastereomers (3.4 g, 86% yield, colourless oil, 95% pure). Subsequent distillation provided an olfactory pure sample.

Source