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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266847Generated: October 25, 2026

Allyl bromide → 3-Allyloxycarbonyl-5-nitrobenzoic acid

https://huagongshe.com/reaction/266847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant5-Nitroisophthalic acidHCID 12069—
Product3-Allyloxycarbonyl-5-nitrobenzoic acidHCID 20655860—

Reaction Steps

5-Nitroisophthalic acid (5 g) was converted to the mono allyl ester using one equivalent of allyl bromide (2 ml) using a similar method to that described in example 1. The required acid (2.7 g) was extracted from the organic phase with aqueous NaHCO3. The organic layer contained the di-allyl ester (2.7 g). The mono acid, 3-allyloxycarbonyl-5-nitrobenzoic acid, was obtained as a white solid. Nmr (CDCl3): 4.87 (d, 2H); 5.3-5.5 (q, 2H); 5.97-6.15 (m, 1H); 9.01 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652233
Source datasetuspto-grants-1997_07
ORD IDord-f3bdd4fedad645b091ab60d0d8d31e33
Source noteuspto-grants-1997_07