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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 344826생성일: 2026년 10월 25일

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

반응식

참여 물질

역할이름HCID투입량
반응물Phenyl isocyanateHCID 7672—
반응물TriethylamineHCID 8471—
반응물Methyl 3-butenoateHCID 77314—
반응물4'-Fluoro-3,3',5-trimethyl-2-(3-nitropropyl)-1,1'-biphenylHCID 54040361—
촉매TriethylamineHCID 8471—
용매TolueneHCID 1140—
생성물Methyl 3-[2-(4'-fluoro-3,3',5-trimethyl[1,1'-biphenyl]-2-yl)ethyl]-4,5-dihydro-5-isoxazoleacetateHCID 5438164471.2%

반응 단계

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

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05053525
출처 데이터셋uspto-grants-1991_10
ORD IDord-aa311eec656c4fe7b866b87122ba700a
출처 메모uspto-grants-1991_10