Реакция #6379

Уравнение реакции

lithium bromide

Water

7-(acetyloxy)-β-chloro-3a,4,5,6,7,7a-hexahydro-δ,3a-dimethyl-1H-indene-3-butanol

p-toluenesulfonyl chloride

→

title compound

7-(acetyloxy)-3-(3-chloro-4-bromo-1-methylbutyl)-3a,4,5,6,7,7a-hexahydro-3a-methyl-1H-indene

Растворители

—

ice water

dichloromethane

pyridine

Условия реакции

Обработка

1. 1
   workup.STIRRINGafter stirring the resulting mixture for 1 hour at room temperature
2. 2
   Другоеthe solvents were removed in vacuo
3. 3
   workup.ADDITIONthe residue diluted with water
4. 4
   Экстракцияextracted with ethyl acetate
5. 5
   ПромывкаThe combined organic extracts were subsequently washed with 1N hydrochloric acid, water, 2N aqueous potassium bicarbonate solution and brine
6. 6
   Другоеdried
7. 7
   ДругоеThe residue obtained
8. 8
   Другоеafter evaporation of the ethyl acetate (weighing 2.10 g)
9. 9
   workup.DISSOLUTIONwas dissolved in 40 mL of N,N-dimethylformamide
10. 10
    ТемператураAfter cooling
11. 11
    Экстракцияextracted with ethyl acetate
12. 12
    ПромывкаThe combined organic extracts were washed several times with water
13. 13
    Другоеdried
14. 14
    Другоеevaporated to dryness
15. 15
    Другоеto give

Методика

A solution of 1.50 g (4.76 mmol) of [3aS-[3(βS*,δR*), 3aα,7β,7aβ]]-7-(acetyloxy)-β-chloro-3a,4,5,6,7,7a-hexahydro-δ,3a-dimethyl-1H-indene-3-butanol in 20 mL of dichloromethane and 20 mL of pyridine was treated at 0° C. and under argon with 4.50 g (23.60 mmol) of p-toluenesulfonyl chloride and then stirred overnight at 0° C. Water (8 mL) was then added and, after stirring the resulting mixture for 1 hour at room temperature, the solvents were removed in vacuo and the residue diluted with water and extracted with ethyl acetate. The combined organic extracts were subsequently washed with 1N hydrochloric acid, water, 2N aqueous potassium bicarbonate solution and brine and dried. The residue obtained after evaporation of the ethyl acetate (weighing 2.10 g) was dissolved in 40 mL of N,N-dimethylformamide and heated under argon at 50° C. with 4.00 g (46.06 mmol) of anhydrous lithium bromide for 17 hours. After cooling, the reaction mixture was diluted with ice water and extracted with ethyl acetate. The combined organic extracts were washed several times with water, dried and evaporated to dryness to give 1.62 g (90% overall yield) of the title compound. 1H NMR (60 MHz, CDCl3) δ0.88 (s, 3H), 1.07 (d, J=6.4 Hz, 3H), 2.03 (s, 3H), 3.60 (br AB q, J=10.2 Hz, Δγ=14.0 Hz, 2H), 5.00 (br m, 1H), 5.33 (br s, 1H) ppm.

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