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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187640Generated: October 30, 2026

Potassium Iodide → Ethyl 7-Bromo-3-(3-(tert.-butoxycarbonylamino)propoxy)-naphthalen-2-carboxylate

https://huagongshe.com/reaction/2187640

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
ReactantN-Boc-3-ChloropropylamineHCID 10932310—
ReactantEthyl 7-bromo-3-hydroxy-2-naphthoateHCID 18476207—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductEthyl 7-Bromo-3-(3-(tert.-butoxycarbonylamino)propoxy)-naphthalen-2-carboxylateHCID 18476258100%

Reaction Steps

A mixture of 3.8 g (12.88 mmol) ethyl 7-bromo-3-hydroxynaphthalen-2-carboxylate, 3.0 g (15.5 mmol) 1-(tert.-butoxycarbonylamino)-3-chloropropane (prepared according to Helv. Chim. Acta 76 (1993), 1644), 2.0 g (14.5 mmol) potassium carbonate, and a catalytic amount of potassium iodide in 20 ml dry DMF was stirred at 90° C. for 6 h. It was poured into water, extracted three times with ethyl acetate, and the combined organic layers were washed three times with water, dried over sodium sulfate, and concentrated in vacuo. The intermediate was purified by chromatography on silica gel with toluene/acetone 9:1 to give 5.8 g (100%) of a yellow oil, which solidified rapidly upon standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410562B1
Source datasetuspto-grants-2002_06
ORD IDord-6b5b9054a9464b6a999f6674ec845ef5
Source noteuspto-grants-2002_06