반응 #1144436
ord-aaafb6d740874c32a1bd59e0e0b2beee
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후처리
- 1온도The mixture was cooled to −70° C. again
- 2workup.STIRRINGstirred for 20 minutes
- 3기타brought to room temperature
- 4세척washed with saturated aqueous solution of sodium chloride
- 5농축concentrated under reduced pressure
- 6세척eluted with 10% ethyl acetate/hexane
- 7기타crystallized from hexane
실험 절차
Then, a solution of 4.4 mmol of lithium diisopropylamide in 2.8 ml of tetrahydrofuran was added dropwise to a solution of 392 mg (2.0 mmol) 1-butyl-5-ethyluracil in 9 ml of tetrahydrofuran under a nitrogen atmosphere at −70° C. and stirred for 70 minutes at −70° C. and further 5 minutes at −25° C. The mixture was cooled to −70° C. again, added with a solution of 567 mg (2.6 mmol) diphenyl disulfide in 3 ml of tetrahydrofuran, stirred for 20 minutes, added with 1 ml of acetic acid, brought to room temperature, washed with saturated aqueous solution of sodium chloride and concentrated under reduced pressure. The residue was adsorbed on a silica gel, eluted with 10% ethyl acetate/hexane and crystallized from hexane to obtain 40 mg of 1-butyl-5-ethyl-6-phenylthiouracil (Yield: 7%).