반응 #1283
ord-c2956910e6964c68a222931d19fd2abc
반응 방정식
반응물
시약
반응 조건
후처리
- 1온도a cooled
- 2기타was continued at 0° until the frothing
- 3기타(about 2.0 hours)
- 4workup.STIRRINGstirred at 0° under argon for 4.0 hours
- 5추출extracted with ethyl acetate (2×100 ml.)
- 6추출extracted with ethyl acetate (3×500 ml.)
- 7세척the combined organic extracts were washed with brine (100 ml.)
- 8건조dried (anhydrous sodium sulfate)
- 9여과filtered
- 10기타evaporated to dryness
- 11기타dried in vacuo
- 12기타The crude product mixture was chromatographed on a silica gel column (Merck)
- 13세척eluting the column with methylene chloride:methanol:acetic acid (100:5:0.2)
- 14기타to give 27.22 g
실험 절차
A solution of N-[(1,1-dimethylethoxy)carbonyl]-L-serine (24.3 g., 0.118 mole) in dry dimethylformamide (25 ml.) was added dropwise over a period of 1.0 hour to a cooled (0°, ice-salt bath) suspension of 60% sodium hydride (10.1 g., 0.25 mole) in dry dimethylformamide (200 ml.) and stirring was continued at 0° until the frothing subsided (about 2.0 hours). The reaction mixture was treated dropwise with 1-fluoro-2-nitrobenzene (14.3 ml., 0.13 mole) over a period of 20 minutes, stirred at 0° under argon for 4.0 hours then poured into ice-water (750 ml.) and extracted with ethyl acetate (2×100 ml.). The aqueous phase was brought to pH 1.0 with 6N hydrochloric acid (70 ml.), extracted with ethyl acetate (3×500 ml.) and the combined organic extracts were washed with brine (100 ml.), dried (anhydrous sodium sulfate), filtered, evaporated to dryness and dried in vacuo. The crude product mixture was chromatographed on a silica gel column (Merck), eluting the column with methylene chloride:methanol:acetic acid (100:5:0.2) to give 27.22 g. of product as a thick yellow syrup; Rf =0.27 (methylene chloride:methanol:acetic acid, 100:5:0.5).