Reacción #1296

Ecuación de reacción

1-bromo-4-chlorobutane

cyclopentanecarboxylic acid

diisopropylamine

n-butyl lithium

→

lithium diisopropylamide

title product

1-(4-Chlorobutyl)cyclopentanecarboxylic acid

Disolventes

tetrahydrofuran

tetrahydrofuran

tetrahydrofuran

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturamaintaining the temperature between -3° C. -1° C
2. 2
   workup.WAITAfter an additional 15 minutes at 0° C.
3. 3
   Otrothe bath was removed
4. 4
   workup.STIRRINGthe reaction stirred 15 minutes more
5. 5
   Otroto rise to 11° C
6. 6
   Otrorising to -66° C
7. 7
   workup.WAITAfter 16 hours
8. 8
   Temperaturato warm to room temperature in situ
9. 9
   OtroThe reaction was quenched with methanol (10 ml.)
10. 10
    Concentraciónconcentrated in vacuo
11. 11
    OtroThe residue was partitioned between water (200 ml.) and ethyl ether (200 ml.)
12. 12
    Extracciónextracted with methylene chloride (3×150 ml.)
13. 13
    Secadodried (magnesium sulfate)
14. 14
    Filtraciónfiltered
15. 15
    Otroevaporated
16. 16
    Otroto give 20.0 g

Procedimiento

A solution of lithium diisopropylamide was prepared under nitrogen from diisopropylamine (31.0 ml., 220 mmol.) and n-butyl lithium (1.5M in hexane, 88.0 ml., 220 mmol.) in tetrahydrofuran (80 ml.), maintaining the temperature between -3° C. -1° C. After stirring 15 minutes, cyclopentanecarboxylic acid (11.4 g., 100 mmol.) in tetrahydrofuran (10 ml.) was added at 0° C.-3° C. over 25 minutes. After an additional 15 minutes at 0° C., the bath was removed and the reaction stirred 15 minutes more, causing the temperature to rise to 11° C. The milky white solution was cooled to -74° C. and 1-bromo-4-chlorobutane (23 ml., 200 mmol.) in tetrahydrofuran was added quickly, the temperature rising to -66° C. After 16 hours, the reaction was allowed to warm to room temperature in situ. The reaction was quenched with methanol (10 ml.) and concentrated in vacuo. The residue was partitioned between water (200 ml.) and ethyl ether (200 ml.). The aqueous layer was acidified to pH 1 with 12M hydrochloric acid and extracted with methylene chloride (3×150 ml.), dried (magnesium sulfate), filtered and evaporated to give 20.0 g. of the title product as a yellow oil.

Fuente