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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040686Generated: October 26, 2026

Potassium Carbonate → 2-(2-Tert-butoxycarbonylaminoethylamino)-6-nitro-benzoic acid methylester

https://huagongshe.com/reaction/1040686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN-BOC-ethylenediamineHCID 187201—
ReactantMethyl 2-fluoro-6-nitrobenzoateHCID 597752—
SolventDimethylformamideHCID 6228—
Product2-(2-Tert-butoxycarbonylaminoethylamino)-6-nitro-benzoic acid methylesterHCID 6726425998.8%

Reaction Steps

To a stirred solution of 2-fluoro-6-nitro-benzoic acid methyl ester (0.35 g, 0.00176 mol) in DMF (8 mL) under nitrogen was added (2-amino-ethyl)-carbamic acid tertbutyl ester (0.28 g, 0.00176 mol) and potassium carbonate (0.49 g, 0.0035 mol). The reaction mixture was stirred at room temperature for 48 h. The reaction solvent was removed and the resulting oil redissolved in ethyl acetate and washed with water. The organic phase was dried over magnesium sulfate, filtered, and concentrated in vacuo. The reaction mixture was purified by ISCO chromatography on silica gel (20 g column) using 10-50% ethyl acetate-hexane to give 2-(2-tert-Butoxycarbonylamino-ethylamino)-6-nitro-benzoic acid methyl ester (0.59 g, 98% yield). 1H NMR (400 MHz, DMSO-d6) δ 7.48 (t, 1H, J=8 Hz), 7.11 (m, 2H), 7.00 (m, 1H), 6.52 (m, 1H), 3.77 (s, 3H), 3.24 (m, 2H), 3.11 (m, 2H), 1.44 (s, 9H); MS (m/e) 340 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552186B2
Source datasetuspto-grants-2013_10
ORD IDord-f79cbeffa538415dbcc2f4742e6267a0
Source noteuspto-grants-2013_10