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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1686997Generated: November 2, 2026

Hydrochloric Acid → 2-(2-Amino-ethylamino)-6-nitro-benzoic acid

https://huagongshe.com/reaction/1686997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-(2-Tert-butoxycarbonylaminoethylamino)-6-nitro-benzoic acidHCID 67264612—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product2-(2-Amino-ethylamino)-6-nitro-benzoic acidHCID 6726469276%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 2-(2-tert-butoxycarbonylamino-ethylamino)-6-nitro-benzoic acid (0.22 g, 0.00068 mol) in THF at 0° C. was added 4N HCl in dioxane (0.68 mL). The reaction was stirred at 0° C. for 2 h then warmed to room temperature overnight. The reaction mixture was diluted with ethyl acetate and washed with water. The organic phase was dried over magnesium sulfate, filtered and concentrated in vacuo to give 2-(2-amino-ethylamino)-6-nitro-benzoic acid (0.12, 76% yield). 1H NMR (400 MHz, CDCl3) δ 11.6 (s, 1H), 7.57 (t, 1H, J=7.6 Hz), 7.05 (d, 1H, J=7.8 Hz), 6.80 (d, 1H, J=7.8 Hz), 4.0 (broad s, 3H), 3.63 (m, 2H), 3.07 (m, 2H); MS (m/e) 226 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08148391B2
Source datasetuspto-grants-2012_04
ORD IDord-7f62ddc8f8904c9580877bb29ea060c1
Source noteuspto-grants-2012_04