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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750160Generated: October 30, 2026

Triethylamine → HCID 23060698, compound

https://huagongshe.com/reaction/750160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,3-Dihydro-1-benzofuran-5-ylmethanamineHCID 2735367—
ReactantHCID 23060590HCID 23060590—
SolventMethanolHCID 887—
ProductHCID 23060698HCID 2306069882.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 6-fluoro-1-oxo-4-phenyl-1H-isochromen-3-carboxylic acid (1 g), 5-aminomethyl-2,3-dihydrobenzo[b]furan (1.1 g), triethylamine (1 ml) and methanol (10 ml) was stirred at 50° C. for 36 hrs. The reaction mixture was concentrated, 1N-hydrochloric acid was added and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. To the residue was added 4N-hydrochloric acid-ethyl acetate solution (5 ml) at room temperature and the mixture was stirred for 12 hrs. The reaction mixture was concentrated under reduced pressure and the residue was purified by recrystallization (ethyl acetate-hexane) to give the title compound (1.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07402595B2
Source datasetuspto-grants-2008_07
ORD IDord-942d0586349b4dd5b391525983cbf885
Source noteuspto-grants-2008_07