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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773573Generated: October 26, 2026

Nitric Acid → 3-Chloro-6-nitrotoluene

https://huagongshe.com/reaction/1773573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
ReactantSulfuric AcidHCID 1118—
Reactant3-ChlorotolueneHCID 7931—
SolventAcetic AcidHCID 176—
Product3-Chloro-6-nitrotolueneHCID 7932939%
Product3-Chloro-4-nitrotolueneHCID 12347814%

Reaction Steps

Concentrated nitric acid (16 mL) was slowly added, at 0° C., to a solution of 3-chlorotoluene (3 mL, 25.4 mmol) and concentrated sulfuric acid (6 mL) in glacial acetic acid (20 mL) and the resulting mixture was stirred for 24 hours allowing the temperature to rise until room temperature. The reaction mixture was then poured into ice-water and partitioned between water and diethyl ether. The aqueous phase was separated and extracted twice with diethyl ether; the combined organic extracts were washed with water and brine, dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure. The yellow oily residue was purified on a silica gel plug and twice by flash chromatography to give 1.22 g (14% yield) of 2-chloro-4-methyl-1-nitro-benzene as a yellow oil and 3.39 g (39% yield) of 4-chloro-2-methyl-1-nitro-benzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255110B2
Source datasetuspto-grants-2016_02
ORD IDord-dc4775633c1d4cd497d84368ba7831d2
Source noteuspto-grants-2016_02