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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969799Generated: October 30, 2026

Hydrochloric Acid → 2-Chloro-6-ethylbenzoic acid

https://huagongshe.com/reaction/969799

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN,N-DimethylanilineHCID 949—
ReactantSulfuric AcidHCID 1118—
ReactantSulfamic AcidHCID 5987—
ReactantChloroformHCID 6212—
ReactantAcetic AnhydrideHCID 7918—
Reactant2-Chloro-6-ethylanilineHCID 13879195—
ReactantSodium NitriteHCID 23668193—
SolventAcetic AcidHCID 176—
Product2-Chloro-6-ethylbenzoic acidHCID 22613769—

Reaction Conditions

Temperature6 °C

Reaction Steps

3.60 g (21.2 mmol) of 2-chloro-6-ethylaniline in 60 ml of acetic acid is introduced into a reaction vessel and the clear, colourless solution is cooled to 6° C. At that temperature, 3.64 g (22.7 mmol) of a 43% aqueous sodium nitrite solution are added and then, in the course of 15 minutes, a solution of 4.32 g (42.4 mmol) of sulfuric acid (96%) in 7 ml of acetic acid is added dropwise. The resulting dark-red solution is then stirred for 30 minutes. When a diazo colour test, for example using dimethylaniline-coated indicator paper, is positive and a colour spot test, e.g. using KI indicator paper moistened with aqueous 1 N hydrochloric acid solution, is negative, 15 mg of sulfamic acid are added and then, at a temperature of 10° C., 8.7 ml (91.6 mmol) of acetic anhydride are added. The reaction mixture is then transferred to a glass autoclave and rinsed with 20 ml of acetic acid. At a temperature of 20° C. the autoclave is flushed out three times with nitrogen and then flushed out three times with CO. 220 mg of Pd2(dba)3.CHCl3 (0.212 mmol) in 5 ml of acetic acid are then metered in using a cannula at a CO pressure of 1 bar, then a CO pressure of 8 bar is applied and the reaction mixture is stirred overnight at 45° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07307175B2
Source datasetuspto-grants-2007_12
ORD IDord-4ad1d74ae2a341349c848e3f2efe025b
Source noteuspto-grants-2007_12