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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263601Generated: October 31, 2026

Allyl bromide → HCID 22168678, compound

https://huagongshe.com/reaction/1263601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
ReactantMonomethyl-5-nitroisophthalateHCID 6931682—
Reactant1-Methyl 3-(2-propen-1-yl) 5-amino-1,3-benzenedicarboxylateHCID 22168580—
SolventDimethylformamideHCID 6228—
ProductHCID 22168678HCID 22168678—

Reaction Steps

Starting material (3(b)) was synthesised as follows. A mixture of mono-methyl-5-nitroisophthalate (13.8 g), allyl bromide (7.96 g), potassium carbonate (13.94 g) and DMF (160 ml) was stirred at ambient temperature for 4.5 h. The solid was filtered and DMF was evaporated away from the filtrate under reduced pressure. The residue was dissolved in diethyl ether (300 ml) and water (100 ml) and stirred for five minutes. The organic layer was separated and washed with saturated sodium bicarbonate solution (220 ml), brine (200 ml). dried over magnesium sulphate and evaporated under reduced pressure to give 5-nitro-isophthalic acid allyl ester methyl ester (3(a)) as a yellow oil (14.74 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541491B1
Source datasetuspto-grants-2003_04
ORD IDord-ccbf443955004c7b845c19a3ee27cb8c
Source noteuspto-grants-2003_04