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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403858Generated: November 4, 2026

Water → Methyl 1-(4-amino-3-bromophenyl)cyclopropanecarboxylate

https://huagongshe.com/reaction/1403858

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 1-(4-aminophenyl)cyclopropane-1-carboxylateHCID 58841079—
SolventAcetonitrileHCID 6342—
ProductMethyl 1-(4-amino-3-bromophenyl)cyclopropanecarboxylateHCID 5912919478.5%

Reaction Steps

To a solution of methyl 1-(4-aminophenyl)cyclopropanecarboxylate (10.38 g, 0.05 mol) in acetonitrile (200 mL) was added NBS (9.3 g, 0.05 mol) at room temperature. The mixture was stirred overnight. Water (200 mL) was added. The organic layer was separated and the aqueous phase was extracted with EtOAc (80 mL×3). The organic layers were dried with anhydrous Na2SO4 and evaporated to give methyl 1-(4-amino-3-bromophenyl)cyclopropanecarboxylate (10.6 g, 78%), which was used directly in the next step. 1H NMR (400 MHz, CDCl3) δ 7.38 (d, J=2.0 Hz, 1H), 7.08 (dd, J=1.6, 8.4 Hz, 1H), 6.70 (d, J=8.4 Hz, 1H), 3.62 (s, 3H), 1.56-1.54 (m, 2H), 1.14-1.11 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912199B2
Source datasetuspto-grants-2014_12
ORD IDord-c8544eff4db146e0bd20704161edb0df
Source noteuspto-grants-2014_12