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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724128Generated: November 2, 2026

3-Nitrophenylboronic Acid → HCID 57560102, compound

https://huagongshe.com/reaction/1724128

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Nitrophenylboronic AcidHCID 1677—
ReactantSodium CarbonateHCID 10340—
ReactantBenzoic acid N'-[3-(2-bromo-phenyl)-propionyl]-N'-isopropyl-hydrazideHCID 57560116—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 57560102HCID 5756010222%

Reaction Steps

A solution of benzoic acid N′-[3-(2-bromo-phenyl)-propionyl]-N′-isopropyl-hydrazide (50 mg, 0.13 mmol) in DME (4 ml)/2M Na2CO3 (225 μL, 0.45 mmol) was treated with 3-nitro-phenylboronic acid (43 mg, 0.26 mmol) and Pd[PPh3]4 (15 mg, 0.013 mmol) for 18 hours at 90° C. The reaction mixture was partitioned between water and dichloromethane. The organic layer was washed with brine, dried over sodium sulfate, filtered, and concentrated. The crude was absorbed on silica and purified on a silica gel column with a 20-50% ethyl acetate/hexanes gradient to afford the product as a solid (12 mg, 22%). LC-MS m/e 432.31 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485752B2
Source datasetuspto-grants-2009_02
ORD IDord-3b781ef619b94cb29e1ffa2543aedc7d
Source noteuspto-grants-2009_02