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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 605536Generated: November 2, 2026

4-Nitrobenzyl bromide → HCID 57565267, compound

https://huagongshe.com/reaction/605536

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzyl bromideHCID 66011—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant1H-indene-3-carboxylic acidHCID 84261—
CatalystPalladiumHCID 23938—
SolventBenzeneHCID 241—
SolventEthanolHCID 702—
ProductHCID 57565267HCID 5756526795%

Reaction Steps

To a solution of 3H-Indene-1-carboxylic acid (2.0 g, 13.3 mmol) in ethanol (35 mL) was added 10% Pd/C (200 mg). The reaction mixture was stirred under an H2 atmosphere for 1 h. The mixture was filtered through Celite and concentrated in vacuo. The residue was combined with p-nitrobenzyl bromide (5.8 g, 26.8 mmoles) and 1,8-diazabicyclo[5.4.0]undec-7-ene (2.4 mL, 16.0 mmol) in 65 mL of benzene, and was stirred at 50° C. for 20 hours. After this period the heterogeneous mixture was gravity filtered and the filtrate was evaporated in vacuo. The residue was combined with CH2Cl2 and was washed with 1N HCl (2×25 mL) and sat'd NaHCO3 (2×25 mL), and the resulting CH2Cl2 solution was dried over anhydrous Na2SO4. The crude solid was purified using flash silica chromatography (0-10% EtOAc/Hexane) to yield 3.61 g (95%) of the intermediate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915253B2
Source datasetuspto-grants-2011_03
ORD IDord-f56bb6e83be84e60b58e0b67fc2c50f6
Source noteuspto-grants-2011_03