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HRID 344826作成日:2026年10月26日

Phenyl isocyanate → Methyl 3-[2-(4'-fluoro-3,3',5-trimethyl[1,1'-biphenyl]-2-yl)ethyl]-4,5-dihydro-5-isoxazoleacetate

https://huagongshe.com/reaction/344826

反応式

関与物質

役割名称HCID仕込み量
反応物Phenyl isocyanateHCID 7672—
反応物TriethylamineHCID 8471—
反応物Methyl 3-butenoateHCID 77314—
反応物4'-Fluoro-3,3',5-trimethyl-2-(3-nitropropyl)-1,1'-biphenylHCID 54040361—
触媒TriethylamineHCID 8471—
溶媒TolueneHCID 1140—
生成物Methyl 3-[2-(4'-fluoro-3,3',5-trimethyl[1,1'-biphenyl]-2-yl)ethyl]-4,5-dihydro-5-isoxazoleacetateHCID 5438164471.2%

反応手順

A solution of 0.1 g (1.0 mmol) of methyl 3-butenoate and 0.174 ml (1.6 mmol) of phenyl isocyanate in 1 ml of toluene was added with stirring to a solution of 0.240 g (0.8 mmol) of the nitropropyl compound from Step D and 2 drops of triethylamine in 1 ml of toluene. The resulting mixture was stirred at room temperature for 3 hours. Additional quantities of methyl 3-butenoate (0.1 ml), triethylamine (0.1 ml) and phenyl isocyanate (0.15 ml) were added successively and stirring was continued overnight (18 hours). The mixture was filtered and the filtrate was concentrated in vacuo to a residue which was purified by flash chromatography on silica gel (230-400 mesh), first being eluted with methylene chloride to remove the impurities. Continued elution with acetone/methylene chloride (1:50, v/v) gave the desired product (0.218 g, 0.57 mmol, 71%) as a pale viscous oil. nmr (CDCl3) δ: 2.28 (6H, s), 2.32 (3H, s), 2.2-3.0 (6H, m), 3.70 (3H, s), 4.6-5.0 (H, m), 6.85 (H, bs), 7.0-7.2 (4H, m). IR (neat) 1735 cm-1

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05053525
出典データセットuspto-grants-1991_10
ORD IDord-aa311eec656c4fe7b866b87122ba700a
出典メモuspto-grants-1991_10