4-Nitrophenol → 4-Nitrophenyl 5-(1-hydroxysilinan-1-yl)pentanoate
反応式
[OH:1][Si:2]1([CH2:8][CH2:9][CH2:10][CH2:11][C:12]([OH:14])=[O:13])[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3]1.C1(N=C=NC2CCCCC2)CCCCC1.[N+:30]([C:33]1[CH:38]=[CH:37][C:36](O)=[CH:35][CH:34]=1)([O-:32])=[O:31]>C(OCC)(=O)C>[OH:1][Si:2]1([CH2:8][CH2:9][CH2:10][CH2:11][C:12]([O:14][C:36]2[CH:37]=[CH:38][C:33]([N+:30]([O-:32])=[O:31])=[CH:34][CH:35]=2)=[O:13])[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3]1参加物
実験手順
To 5-(1-hydroxysilinan-1-yl)pentanoic acid (130 mg, 0.601 mmol) in ethyl acetate (5 mL), N,N′-dicyclohexylcarbodiimide (186 mg, 0.901 mmol) was added. The reaction was stirred under nitrogen at ambient temperature for 30 minutes. After this time, 4-nitrophenol (100 mg, 0.719 mmol) was added, and the reaction was stirred for 16 hours at ambient temperature. After this time, the reaction was filtered to remove any solids, the filter cake was washed with ethyl acetate, and the filtrate was concentrated under reduced pressure. The residue obtained was purified by silica gel column chromatography eluting with hexanes to 1:3 ethyl acetate/hexanes to afford 4-nitrophenyl 5-(1-hydroxysilinan-1-yl)pentanoate (106 mg, 52%) as a colorless oil. 1H NMR (500 MHz, CDCl3) δ 8.26 (dt, J=9.0, 2.5 Hz, 2H), 7.27 (dt, J=9.0, 2.5 Hz, 2H), 2.61 (t, J=7.5 Hz, 2H), 1.84-1.78 (m, 2H), 1.76-1.67 (m, 4H), 1.56-1.44 (m, 4H), 1.40-1.33 (m, 1H), 0.75-0.63 (m, 6H).
後処理
- stirringthe reaction was stirred for 16 hours at ambient temperature
- filtrationAfter this time, the reaction was filtered
- customto remove any solids
- washthe filter cake was washed with ethyl acetate
- concentrationthe filtrate was concentrated under reduced pressure
- customThe residue obtained
- customwas purified by silica gel column chromatography
- washeluting with hexanes to 1:3 ethyl acetate/hexanes
出典と根拠
- ORDレコード
- ord-b82b652907004f7ab9716277ee08c3f5
- 出典データセット
- uspto-grants-2016_05
- 特許番号
- US09352049B2
反応ノート
読み込み中…