4-Methyl-2-nitrophenol → Ethyl 2-methyl-2-(4-methyl-2-nitrophenoxy)propanoate
反応式
[N+:1]([C:4]1[CH:9]=[C:8]([CH3:10])[CH:7]=[CH:6][C:5]=1[OH:11])([O-:3])=[O:2].[H-].[Na+].Br[C:15]([CH3:22])([CH3:21])[C:16]([O:18][CH2:19][CH3:20])=[O:17].[OH-].[Na+]>CN1CCCN(C)C1=O.C(OCC)(=O)C>[CH3:21][C:15]([O:11][C:5]1[CH:6]=[CH:7][C:8]([CH3:10])=[CH:9][C:4]=1[N+:1]([O-:3])=[O:2])([CH3:22])[C:16]([O:18][CH2:19][CH3:20])=[O:17]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
A solution of 2-nitro-4-methylphenol (11.48 g) in 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone (DMPU) (50 ml) was cooled at 5° C. and treated with portions of sodium hydride (55% w/w dispersion in mineral oil, 3.27 g). The mixture was stirred at room temperature for 2 hours, then cooled to 5° C. and treated with ethyl 2-bromo-2-methylpropionate (13.15 g). The mixture was heated at about 100° C. for 18 hours, then cooled to room temperature and poured into a mixture of aqueous sodium hydroxide solution (1M) and ethyl acetate. The organic solution was separated and washed twice with 1M sodium hydroxide solution, then dried (MgSO4) and concentrated. The resulting oil was purified by flash column chromatography, eluting with a mixture of ethyl acetate and hexane, (increasing from 5:95 v/v to 10:90 v/v), to give ethyl 2-methyl-2-(2-nitro-4-methylphenoxy)propionate (4.48 g) as an oil; NMR: 1.25 (3H, t), 1.60(6H, s), 2.35(3H, s), 4.25(2H, q) and 6.8-7.6(3H, m).
後処理
- temperaturecooled to 5° C.
- temperatureThe mixture was heated at about 100° C. for 18 hours
- temperaturecooled to room temperature
- customThe organic solution was separated
- washwashed twice with 1M sodium hydroxide solution
- dry with materialdried (MgSO4)
- concentrationconcentrated
- customThe resulting oil was purified by flash column chromatography
- washeluting with a mixture of ethyl acetate and hexane, (increasing from 5:95 v/v to 10:90 v/v),
出典と根拠
- ORDレコード
- ord-45dd9e86968a45b98eddc8fc4b0e86f0
- 出典データセット
- uspto-grants-1991_10
- 特許番号
- US05053415
反応ノート
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