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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20943Generated: October 25, 2026

Butyl nitrite → 3-(Dipropylcarbamoyl)benzoic acid

https://huagongshe.com/reaction/20943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl nitriteHCID 10996—
ReactantN-Boc-cis-4-hydroxy-D-prolineHCID 688616—
Reactant3-Bromo-5-(methoxycarbonyl)benzoic acidHCID 22593641—
Reactant(4R)-1-Boc-4-(2-propen-1-yloxy)-D-prolineHCID 67315699—
CatalystCopper bromide (CuBr2)HCID 24611—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product3-(Dipropylcarbamoyl)benzoic acidHCID 18276997%

Reaction Steps

Step G (2): 3-bromo-5-(methoxycarbonyl)benzoic acid. To a mixture of copper (II) bromide (5.5 g, 24.6 mmol), n-butyl nitrite (3.17 g, 30.75 mmol) and acetonitrile (300 mL) was added 3-amino-5-(methoxycarbonyl)benzoic acid (Step G (1), 4.0 g, 20.5 mmol) in aceonitrile (300 mL) over 30 min at 0° C. and the mixture was warmed up and stirred at rt for 3 h. H2O was added and acetonitrile was removed. Ethyl acetate (600 mL) was added and the mixture was washed with 3N HCl, H2O, dried over Na2SO4, and concentrated in vacuo to give the title compound (97% yield): 1H NMR (CDCl3, 500 MHz) δ ppm 3.96 (3H, s), 8.41 (1H, s), 8.41 (1H, s), 8.67 (1H, m). MS (ESI) (M−H)− 259.02.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745470B2
Source datasetuspto-grants-2010_06
ORD IDord-f1e12c8ab4c14f8c9ebf66d37ccca20b
Source noteuspto-grants-2010_06