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HRID 2064075作成日:2026年10月25日

Isopropanol → 2-Fluoro-4-isopropoxy-1-nitrobenzene

https://huagongshe.com/reaction/2064075

反応式

関与物質

役割名称HCID仕込み量
反応物IsopropanolHCID 3776—
反応物Di-tert-butyl azodicarboxylateHCID 97268—
反応物3-Fluoro-4-nitrophenolHCID 520948—
反応物2-PyridyldiphenylphosphineHCID 621893—
反応物Ether hydrochlorideHCID 10953452—
溶媒TetrahydrofuranHCID 8028—
生成物2-Fluoro-4-isopropoxy-1-nitrobenzeneHCID 1353865269.3%

反応手順

A mixture of 5-fluoro-4-nitrophenol (314 mg, 2.0 mmol), propan-2-ol (120 mg, 2.0 mmol), diphenyl-2-pyridylphosphine (789 mg, 3.0 mmol) and di-tert-butyl azodicarboxylate (691 mg, 3.0 mmol) in tetrahydrofuran (15 ml) was stirred at room temperature under argon for 22 hrs. The mixture was treated with 1M HCl/diethyl ether (15 ml) and stirred at room temperature for 2 hrs, then concentrated under vacuum and the residue dissolved in diethyl ether (10 ml), treated with 5M HCl acid and stirred for 2 hrs. The organic layer was separated, washed with 5M HCl acid (15 ml), then 10% Na2CO3 solution (2×10 ml), dried (MgSO4) and concentrated under vacuum. The residue was purified by chromatography on silica gel eluting with 5-70% ethyl acetate/60-80 petrol ether to afford the title compound as a yellow oil (276 mg, 69%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08288413B2
出典データセットuspto-grants-2012_10
ORD IDord-a4066224525d4eabbcd421d089daec3a
出典メモuspto-grants-2012_10