تفاعل #571325

معادلة التفاعل

lithium bis(trimethylsilyl)amide

3-(4-bromobutyl)-4-thiazolidinone

1,5-diiodopentane

→

solid

المردود 63.8%

3-(4-Bromobutyl)-1-thia-3-azaspiro[5.4]decan-4-one

المردود 63.8%

المذيبات

—

hexanes

THF

ظروف التفاعل

المعالجة

1. 1
   درجة الحرارةwas maintained at or below -55° C
2. 2
   workup.ADDITIONThe addition
3. 3
   درجة الحرارةwarmed to 0° C. with the aid of an ice bath
4. 4
   workup.STIRRINGThe mixture was stirred for additional 20 minutes
5. 5
   أخرىquenched with 500 ml of 0.5N HCl solution
6. 6
   أخرىto remove some of the THF
7. 7
   استخلاصextracted with ether (350 ml, 2×250 ml)
8. 8
   غسيلThe combined extracts were washed successively with water (400 ml) and brine (400 ml)
9. 9
   تجفيفdried with Na2SO4
10. 10
    تركيزconcentrated to a liquid
11. 11
    أخرىThe liquid was chromatographed (2 silica gel columns)

الإجراء التجريبي

To a solution of 3-(4-bromobutyl)-4-thiazolidinone (25 g) in THF (350 ml) cooled to -60° C. was added 1,5-diiodopentane (100 g), and the resultant slurry was cooled to -65° C. A solution of lithium bis(trimethylsilyl)amide (0.220 mole) in hexanes (220 ml) was added dropwise, during which the internal temperature was maintained at or below -55° C. The addition was complete within 30 minutes. The mixture was stirred for additional 15 minutes at the same temperature and thereafter warmed to 0° C. with the aid of an ice bath. The mixture was stirred for additional 20 minutes and thereafter quenched with 500 ml of 0.5N HCl solution. The resultant mixture was placed under vacuum to remove some of the THF and thereafter extracted with ether (350 ml, 2×250 ml). The combined extracts were washed successively with water (400 ml) and brine (400 ml), dried with Na2SO4 and concentrated to a liquid. The liquid was chromatographed (2 silica gel columns) using 20-60% ethyl acetate/hexane as an eluent to obtain about 20.5 g of solid product.

المصدر