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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852608Generated: October 29, 2026

Bromine → Ethyl 4-amino-3-bromo-5-nitrobenzoate

https://huagongshe.com/reaction/852608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantBenzoic acid, 4-amino-3-nitro-, ethyl esterHCID 3018687—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-amino-3-bromo-5-nitrobenzoateHCID 301907994%

Reaction Steps

To a solution of ethyl 4-amino-3-nitrobenzoate (D212) (21.0 g, 100 mmol, 1 equiv) in CH2Cl2 (500 ml) at room temperature was added bromine (6.7 ml, 130 mmol, 1.3 equiv) and the resulting mixture was refluxed for 4 h then bromine (2 ml, 40 mmol, 0.4 equiv) was added and the resulting mixture refluxed for another 3 h then cooled to room temperature. The organic phase was washed twice with a 10% aqueous Na2S2O3 solution and twice with H2O, dried over MgSO4 and concentrated in vacuo to give ethyl 4-amino-3-bromo-5-nitrobenzoate (D213) (27.1 g, 94%) as a yellow solid which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253198B2
Source datasetuspto-grants-2007_08
ORD IDord-79ed2912926646e2a2f3706c971546e4
Source noteuspto-grants-2007_08