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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188928Generated: October 30, 2026

Methyl 3-bromo-5-nitrobenzoate → Methyl 3-amino-5-bromobenzoate

https://huagongshe.com/reaction/2188928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-bromo-5-nitrobenzoateHCID 239341—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductMethyl 3-amino-5-bromobenzoateHCID 1876342098.4%

Reaction Steps

To a stirred solution of methyl 3-bromo-5-nitrobenzoate (1.0 g, 3.8 mmol) in methanol (30 mL) was added NiCl2.6H2O (1.8 g, 7.6 mmol) and NaBH4 (430 mg, 11 mmol) successively at 0° C. The reaction mixture was stirred for 30 seconds and was then quenched by the addition of water. The mixture was extracted with ethyl acetate (30 mL×3). The combined organic layers were washed with brine and water, dried over anhydrous Na2SO4, and concentrated under vacuum to afford methyl 3-amino-5-bromobenzoate (860 mg, 97% yield). 1H NMR (400 MHz, d-DMSO) δ 7.14 (dd, J=2.0, 2.4 Hz, 1H), 7.11 (t, J=2.4 Hz, 1H), 6.94 (t, J=2.8 Hz, 1H), 5.72 (brs, 2H), 3.79 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324207B2
Source datasetuspto-grants-2012_12
ORD IDord-1f0c05ffe10a45788882b5420f6a5e8f
Source noteuspto-grants-2012_12