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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfamic Acid | HCID 5987 | — |
| Reactant | 2,6-Diethyl-p-toluidine | HCID 90536 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Chloro-2,6-diethyl-4-methylbenzene | HCID 59488982 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08334417B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-ae868bfcd0d74c5496488982e9cf5050 |
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| Source note | uspto-grants-2012_12 |
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