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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036795Generated: October 30, 2026

Tetrahydrofuran → HCID 3136484, compound

https://huagongshe.com/reaction/2036795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantGlycine ethyl esterHCID 12176—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Bromo-5-(chloromethyl)pyridineHCID 11701259—
SolventEthyl AcetateHCID 8857—
ProductHCID 3136484HCID 313648433%

Reaction Steps

A solution of 5-bromonicotinic acid (4 g, 0.02 mol) in thionyl chloride (25 mL) was heated under reflux for 4 h. The excess thionyl chloride was removed under reduced pressure to provide 5-bromonicotinyl chloride which was used without further purification. To 5-bromonicotinyl chloride (3.5 g, 13.6 mmol) was added glycine ethylester (2.1 g, 20.3 mmol) and diisopropyl ethyl amine (2.6 g, 20.1 mmol) in THF (70 mL) and the reaction mixture stirred at RT for 16 h. The reaction mixture was diluted with EtOAc and washed with brine solution. The combined organic layers were dried over Na2SO4, filtered and concentrated under reduced pressure and the residue was purified by silica gel column chromatography using 25% EtOAc in hexane to provide ethyl 2-(5-bromonicotinamido)acetate 1.2 g (33%) as a brown solid. LCMS Method T: retention time 1.28 min; [M+1]=288.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575184B2
Source datasetuspto-grants-2013_11
ORD IDord-971f8e6155c04376ab01892a9f45683e
Source noteuspto-grants-2013_11