반응 #61780
ord-0d51bfc3522e4ff88dd390dfc9b21c68
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시약
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후처리
- 1온도The mixture was cooled to 0° C.
- 2workup.STIRRINGThe mixture was stirred overnight at room temperature (r.t.)
- 3온도cooled to 0° C
- 4workup.STIRRINGstirring
- 5workup.WAITcontinued for 60 min
- 6여과Precipitated salts were filtered off
- 7세척washed with THF
- 8기타The combined THF-solutions were evaporated
- 9추출the residue extracted twice with ethyl acetate
- 10건조The organic phase was dried (sodium sulphate)
- 11기타evaporated
- 12기타The orange resin crystallized after a short time
- 13workup.STIRRINGwas stirred with ethyl acetate/n-heptane 1:3
- 14기타isolated by filtration
- 15세척washed with tert-butyl-methyl ether
- 16기타dried
- 17기타The combined mother liquor from the washings was evaporated
- 18workup.ADDITIONthe crystalline precipitate treated as above
실험 절차
4.67 g (123 mmol) lithium aluminium hydride was suspended in 220 ml tetrahydrofuran (THF) and stirred for 20 min. at room temperature. The mixture was cooled to 0° C. and a solution of 15.95 g (61.5 mmol) 6-(4-Fluoro-phenyl)-2-methyl-nicotinic acid ethyl ester (WO 03/068749) in 100 ml added within 15 min. at the same temperature. The mixture was stirred overnight at room temperature (r.t.) and cooled to 0° C. 200 ml of saturated sodium chloride solution were added drop by drop and stirring continued for 60 min. Concentrated HCl was added carefully to adjust the pH to 5. Precipitated salts were filtered off and washed with THF. The combined THF-solutions were evaporated and the residue extracted twice with ethyl acetate. The organic phase was dried (sodium sulphate) and evaporated. The orange resin crystallized after a short time, was stirred with ethyl acetate/n-heptane 1:3, isolated by filtration, washed with tert-butyl-methyl ether and dried. The combined mother liquor from the washings was evaporated and the crystalline precipitate treated as above. The combined yield was 9.25 g (69%) of pale yellow powder.