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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241966Generated: October 29, 2026

Tert-butyl 4-chloro-3-nitrobenzoate → Tert-butyl 4-(ethylamino)-3-nitrobenzoate

https://huagongshe.com/reaction/1241966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-chloro-3-nitrobenzoateHCID 10611184—
ReactantEthylamine tetrahydrofuranHCID 66726184—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(ethylamino)-3-nitrobenzoateHCID 20626666100.4%

Reaction Conditions

Temperature65 °C

Reaction Steps

4-Chloro-3-nitrobenzoic acid tert-butyl ester (3.0 g, 11.6 mmol), prepared according to a published procedure [WO 9707101], was cautiously added to a solution of 2.0 M EtNH2/THF (20 mL, 40 mmol) and TEA (2.0 mL, 14 mmol) in anhydrous THF (30 mL). The resulting mixture was heated at 65° C. for 3 h, cooled, concentrated under reduced pressure, diluted with DCM (200 mL), washed with water (2×100 mL) and brine (50 mL), dried over anhydrous Na2SO4 and concentrated to give the title compound (3.1 g, 99%) as a yellow solid, which was used without further purification. 1H-NMR (CDCl3): δ 8.80 (1H, d), 8.24 (1H, br s), 8.02 (1H, dd), 6.84 (1H, d), 3.41 (2H, m), 1.59 (9H, s), 1.40 (3H, t).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115640B2
Source datasetuspto-grants-2006_10
ORD IDord-4d9f744c303c4972beaa8673c09d0d6d
Source noteuspto-grants-2006_10