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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-BOC-ethylenediamine | HCID 187201 | — |
| Reactant | Methyl 2-fluoro-6-nitrobenzoate | HCID 597752 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-Tert-butoxycarbonylaminoethylamino)-6-nitro-benzoic acid methylester | HCID 67264259 | 98.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08552186B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-f79cbeffa538415dbcc2f4742e6267a0 |
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| Source note | uspto-grants-2013_10 |
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