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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580936Generated: October 30, 2026

2-Chloro-4-nitrobenzoic acid → 2-(1,3-Dimethoxy-1,3-dioxopropan-2-yl)-4-nitrobenzoic acid

https://huagongshe.com/reaction/580936

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-4-nitrobenzoic acidHCID 7448—
ReactantDimethyl malonateHCID 7943—
ReactantSodium MethoxideHCID 10942334—
Catalystcopper(I) bromideHCID 24593—
Product2-(1,3-Dimethoxy-1,3-dioxopropan-2-yl)-4-nitrobenzoic acidHCID 10590078—

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution of 2-chloro-4-nitrobenzoic acid (75 g, 372 mmol) in dimethyl malonate (900 mL) was sparged with nitrogen for 15 min. Sodium methoxide (48.3 g, 894 mmol) was added in one portion and the contents exothermed to 480° C. Fifteen minutes later, copper (I) bromide (5.4 g, 37 mmol) was added in one portion and the contents heated to 70° C. for 24 hrs. The reaction was 70% complete by nmr, the contents heated to 85° C. for 6 hrs to completely consume the 2-chloro-4-nitrobenzoic. Water (900 mL) was added to the cooled reaction followed by hexanes (900 mL). The aqueous layer was separated, toluene (900 mL) added, filtered through celite, and aqueous layer separated. Fresh toluene (1800 mL) was added to the aqueous layer and the biphasic mixture acidified with 6N aqueous HCl (90 mL). A white precipitate formed and the contents stirred for 18 hrs. The product was filtered off and dried to give a white soid (78.1 g, 70%) mp=153° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05919795
Source datasetuspto-grants-1999_07
ORD IDord-53ca45c7bf1f45ef8786d2aa0bee8b5b
Source noteuspto-grants-1999_07