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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350921Generated: October 29, 2026

Dipropylamine → Methyl 3-bromo-5-(dipropylcarbamoyl)benzoate

https://huagongshe.com/reaction/1350921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDipropylamineHCID 8902—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Reactant3-Bromo-5-(methoxycarbonyl)benzoic acidHCID 22593641—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-bromo-5-(dipropylcarbamoyl)benzoateHCID 21939662—

Reaction Steps

Carbonyl diimidazole (3–0 g, 18 mmol) is added to a solution of 3-bromo-5-(methoxycarbonyl)benzoic acid (XIX, PREPARATION 2, 3.9 g, 15 mmol) in THF (30 mL). The mixture is stirred for 0.5 hours. Dipropylamine (AMINE, 4.2 mL, 30 mmol) is added to the mixture, which is then stirred for 24 hours. The solvent is then removed under reduced pressure and the mixture is partitioned between ethyl acetate and water. The organic phase is then washed with saline, dried over anhydrous magnesium sulfate, filtered, and concentrated. Column chromatography (silica gel; ethyl acetate/hexanes, 15/85) gives the title compound, IR (diffuse reflectance) 2968, 2958, 1714, 1637, 1479, 1440, 1422, 1321, 1310, 1288, 1273, 1252, 889, 772 and 718 cm−1; NMR (300 MHz, CDCl3) δ 8.21, 7.96, 7.70, 3.95, 3.46, 3.15, 1.69, 1.57, 1.00 and 0.78; MS (ESI+) for C15H20BrNO3 m/z (M+H)+=344.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214715B2
Source datasetuspto-grants-2007_05
ORD IDord-79477274e3dd4903b95d1934ef2a8ab4
Source noteuspto-grants-2007_05