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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2195029Generated: November 1, 2026

Hydrochloric Acid → 1-Chloro-2,6-diethyl-4-methylbenzene

https://huagongshe.com/reaction/2195029

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfamic AcidHCID 5987—
Reactant2,6-Diethyl-p-toluidineHCID 90536—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product1-Chloro-2,6-diethyl-4-methylbenzeneHCID 59488982—

Reaction Conditions

Temperature50 °C

Reaction Steps

To an initial charge of 65 ml of 36% aqueous HCl are added, in portions, 16.33 g [0.1 mol] of 2,6-diethyl-4-methylaniline. The resulting thick suspension is stirred at 50° C. for 5 minutes. It is then cooled to −10° C., and a solution of 8 g [0.116 mol] of NaNO2 in 35 ml of water is added dropwise within approx. 1 h at such a rate that the temperature does not exceed −5° C. 80 mg of sulphamic acid are added. Then the suspension of the diazonium salt, cooled to −10° C., is metered within about 30 minutes into a solution, heated to 65° C., of 4.18 g [0.025 mol] of FeCl3 in 65 ml of 36% aqueous HCl. The reaction mixture is then stirred at 65° C. for another 1 hour, allowed to cool to room temperature and admixed with 200 ml of water, the phases are separated and the aqueous phase is extracted three times with 50 ml each time of methylene chloride. The combined organic phases are washed twice with 25 ml each time of water, dried and concentrated under reduced pressure. This gives 17.9 g of an oil which, according to GC, contains 93.1% 2,6-diethyl-4-methylchlorobenzene (91% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334417B2
Source datasetuspto-grants-2012_12
ORD IDord-ae868bfcd0d74c5496488982e9cf5050
Source noteuspto-grants-2012_12