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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375655Generated: October 31, 2026

Triethylamine → 5-(3-(3-Oxo-butyl)-phenyl)-isoxazole-3-carboxylic Acid Methyl Ester

https://huagongshe.com/reaction/1375655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Buten-2-olHCID 11716—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantMethyl 5-(3-bromophenyl)isoxazole-3-carboxylateHCID 53393795—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Product5-(3-(3-Oxo-butyl)-phenyl)-isoxazole-3-carboxylic Acid Methyl EsterHCID 6950809659.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of 5-(3-Bromo-phenyl)-isoxazole-3-carboxylic acid methyl ester (1.5 g, 5.3 mmol), Pd(OAc)2 (60 mg, 0.27 mmol), P(o-tolyl)3 (162 mg, 0.53 mmol) in anhydrous N,N-dimethylformamide (15 mL) in a pressure tube was added 3-buten-2-ol (0.92 mL, 10.6 mmol) and triethylamine (1.1 mL, 7.95 mmol). The mixture was flushed with nitrogen for 3 minutes, capped and heated to 100° C. for 30 minutes. The reaction mixture was allowed to cool to ambient temperature, partitioned between ethyl acetate and water (75 mL, 1:1). The organic layer was washed with brine (2×25 mL), dried (Na2SO4), filtered, concentrated under reduced pressure and purified on a Silica Gel MPLC eluting with 20–40% ethyl acetate/hexanes to provide the titled compound as a light yellow solid (860 mg, 59%). MS (ESI(+)) m/e 274 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169797B2
Source datasetuspto-grants-2007_01
ORD IDord-93c2b8de9d8549a5bef97182f8516e1d
Source noteuspto-grants-2007_01