2-Nitropropane → 3-Methyl-1-(methylsulfonyl)-3-nitrobutane

HRID 1056208

반응식

HRID 1056208 반응식
[CH3:1][S:2]([CH:5]=[CH2:6])(=[O:4])=[O:3].N1CCCN2CCCCCC=12.[N+:18]([CH:21]([CH3:23])[CH3:22])([O-:20])=[O:19]>>[CH3:22][C:21]([N+:18]([O-:20])=[O:19])([CH3:23])[CH2:6][CH2:5][S:2]([CH3:1])(=[O:4])=[O:3]

참가 물질

4

반응물 3

HCID 3982-NitropropaneHCID 19354Methyl vinyl sulfoneHCID 811841,8-Diazabicyclo(5.4.0)undec-7-ene

생성물 1

HCID 897822733-Methyl-1-(methylsulfonyl)-3-nitrobutane수율 73%

실험 절차

A solution of (methylsulfonyl)ethene (1.51 mL, 17.24 mmol, Sigma-Aldrich) and 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine (3.86 ml, 25.9 mmol) in 2-nitropropane (72.8 mL, 810 mmol, Sigma-Aldrich) was stirred at RT for 2 d. The crude product was adsorbed onto silica and was purified via automated flash chromatography (silica gel) with 100% DCM followed by 1% 2 M NH3 in MeOH/DCM to give 3-methyl-1-(methylsulfonyl)-3-nitrobutane (338a, 2.45 g, 12.55 mmol, 73% yield) as a white solid. 1H NMR (400 MHz, DEUTERIUM OXIDE) δ ppm 1.31 (s, 6H) 2.08 (d, J=17.02 Hz, 1H) 2.08 (dd, J=4.30, 3.52 Hz, 1H) 3.05 (s, 3H) 3.33 (d, J=17.02 Hz, 1H) 3.33 (t, J=3.91 Hz, 1H).

후처리

  1. customwas purified

출처 및 근거

ORD 기록
ord-4f20479f3707466cb3cb5ebdd8df39d0
출처 데이터셋
uspto-grants-2016_07
특허 번호
US09394297B2

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