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HRID 1768404作成日:2026年10月25日

Formaldehyde → 2-(2-Nitrophenyl)propan-1-ol

https://huagongshe.com/reaction/1768404

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物1-Ethyl-2-nitrobenzeneHCID 69156—
反応物Potassium tert-butoxideHCID 23665647—
溶媒Dimethyl SulfoxideHCID 679—
溶媒tert-ButanolHCID 6386—
生成物2-(2-Nitrophenyl)propan-1-olHCID 1138975589%

反応手順

1-Ethyl-2-nitrobenzene (13.5 mL, 100 mmol) was dissolved in dimethylsulfoxide (100 mL). Paraformaldehyde (4.50 g, 150 mmol) and KOtBu (2.81 g, 25 mmol) in t-butyl alcohol (30 mL) were added and the mixture was stirred at room temperature for 3 h. The solution was washed with a molar solution of HCl (25 mL), followed by brine (3×100 mL). All the aqueous layers were combined and extracted with ethyl acetate(3×100 mL). The organic portion was dried (MgSO4), filtered and the solvent was removed in vacuo. The crude product was purified on a silica gel column. Elution of the column with 20-30% ethyl acetate in hexanes gave 16.12 g (89 mmol, 89% yield) of 2-(2-nitrophenyl)propanol. 1H-NMR (600 MHz, DMSO-d6): δ 7.75 (d, J=8.10 Hz, 1H, Ar—H), 7.63 (t, J=7.62 Hz, 1H, Ar—H), 7.58 (d, J =7.80 Hz, 1H, Ar—H), 7.42 (t, J=7.50, 1H, Ar—H), 4.73 (t, J=5.30 Hz, 1H, OH), 3.50 (m, 2H, CH 2), 3.19 (m, 1H, CH), 1.21 (d, J=6.90 Hz, 3H, CH3). TLC: 20% ethyl acetate in hexane, Rf=0.3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07235670B2
出典データセットuspto-grants-2007_06
ORD IDord-c5fd3362a8c940c89bca1510ba9636dd
出典メモuspto-grants-2007_06