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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350333Generated: October 26, 2026

Benzyl Bromide → 1,3-Dibenzyl 5-nitrobenzene-1,3-dicarboxylate

https://huagongshe.com/reaction/1350333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Nitroisophthalic acidHCID 12069—
SolventDimethylformamideHCID 6228—
Product1,3-Dibenzyl 5-nitrobenzene-1,3-dicarboxylateHCID 1906392676.7%

Reaction Steps

In DMF (60 mL) was stirred 5-nitro-1,3-benzenedicarboxylic acid (2.1 g, 10 mmol) and potassium carbonate (8.3 g, 60 mmol). To this was added benzyl bromide (3.60 g, 21 mmol) and the mixture stirred at room temperature for 18 hours. The mixture was then filtered free of solids and the DMF solution evaporated at reduced pressure to give an oil. The oil was partitioned between methylene chloride (100 mL) and 10% citric acid solution (100 mL). The organic phase was separated, washed successively with saturated sodium bicarbonate solution (100 mL) and then brine (100 mL). The organic phase was dried over magnesium sulfate and evaporated at reduced pressure to give 1.5 g (39%) of the solid diester. MS: M-benzyl=300.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214712B2
Source datasetuspto-grants-2007_05
ORD IDord-59228f2f3df94d35acdd9a5969d726f3
Source noteuspto-grants-2007_05