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HRID 344826Erstellt: 24. Oktober 2026

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/de/reaction/344826

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenyl isocyanateHCID 7672—
EduktTriethylamineHCID 8471—
EduktMethyl 3-butenoateHCID 77314—
Edukt4'-Fluoro-3,3',5-trimethyl-2-(3-nitropropyl)-1,1'-biphenylHCID 54040361—
KatalysatorTriethylamineHCID 8471—
LösungsmittelTolueneHCID 1140—
ProduktMethyl 3-[2-(4'-fluoro-3,3',5-trimethyl[1,1'-biphenyl]-2-yl)ethyl]-4,5-dihydro-5-isoxazoleacetateHCID 5438164471,2%

Reaktionsschritte

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

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05053525
Quelldatensatzuspto-grants-1991_10
ORD IDord-aa311eec656c4fe7b866b87122ba700a
Quellennotizuspto-grants-1991_10