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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384753Generated: October 27, 2026

Nitric Acid → Methyl 5-(3-chloropropoxy)-4-methoxy-2-nitrobenzoate

https://huagongshe.com/reaction/384753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantMethyl 3-(3-chloropropoxy)-4-methoxybenzoateHCID 11623039—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
ProductMethyl 5-(3-chloropropoxy)-4-methoxy-2-nitrobenzoateHCID 1166663161%

Reaction Steps

The aforementioned J. Med. Chem., 44, 3965 (2001) further describes a process for preparing a 4-alkoxy-5-halogenoalkoxy-2-nitrobenzoic acid compound from a 4-alkoxy-3-hydroxybenzoic acid compound. For example, methyl 3-hydroxy-4-methoxybenzoate is reacted with 3-chloropropyl p-toluenesulfonate in an aqueous potassium carbonate solution in the presence of tricaprylmethyl ammonium chloride to produce methyl 3-(3-chloropropoxy)-4-methoxybenzoate, and the methyl 3-(3-chloropropoxy)-4-methoxybenzoate is reacted with 70% nitric acid in a mixture of dichloromethane and acetic acid, to give methyl 5-(3-chloropropoxy)-4-methoxy-2-nitrobenzoate in 61% yield (based on the amount of methyl 3-hydroxy-4-methoxybenzoate).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367824B2
Source datasetuspto-grants-2013_02
ORD IDord-4b5963af7db3486097dc577675640531
Source noteuspto-grants-2013_02