반응 #1687623
ord-1432d4615d12405b801552a31d08a4bd
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후처리
- 1기타prepared from 57 by the procedure
- 2기타Evaporation in vacuo
- 3기타give a red oil which
- 4추출Extraction with 4×100 ml of dichloromethane
- 5건조drying of the organic phase over magnesium sulfate, and evaporation in vacuo
- 6기타gave a red oil
- 7여과Filtration and evaporation
실험 절차
A suspension of 6.3 g (0.020 mol) of the methiodide of 57 (prepared from 57 by the procedure described in Example 1) in 75 ml of methanol was cooled to -10° C., and 1.0 g (0.026 mol) of sodium borohydride was added. When the gas evolution had ceased, the mixture was stirred for 3 h at room temperature. Evaporation in vacuo give a red oil which was dissolved in 100 ml of a saturated sodium chloride solution. Extraction with 4×100 ml of dichloromethane, drying of the organic phase over magnesium sulfate, and evaporation in vacuo gave a red oil. The oil was dissolved in 50 ml of ether and stirred with charcoal. Filtration and evaporation gave the base of 59 as a colorless oil, 58. Yield: 1.6 g (0.009 mol, 45%). A 0.5 g portion of 58 was converted to the title compound. M.P. 181°-183° C. Anal. (C11H16N4O2) C, H, N.