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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977349Generated: November 1, 2026

Allyl bromide → HCID 22168678, compound

https://huagongshe.com/reaction/1977349

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 numberUS06232338B1
Source datasetuspto-grants-2001_05
ORD IDord-4bc15af671fc4e71bdc3fa40bd35db5e
Source noteuspto-grants-2001_05