HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636362Generated: October 27, 2026
Water → 2,3-Dichloro-6-nitrobenzyl chloride
https://huagongshe.com/reaction/636362
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (2,3-Dichloro-6-nitrophenyl)methanol | HCID 11160370 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,3-Dichloro-6-nitrobenzyl chloride | HCID 9834663 | — |
Reaction Steps
Under nitrogen, 27.9 mL of triethylamine was added to the concentrated solution of 2,3-dichloro-6-nitrobenzylalcohol prepared in the previous step. To this solution, 14.6 mL of thionyl chloride was added via an addition funnel over 15 minutes. Following addition, the solution is heated to 45-50° C. for 18 hours, then cooled to room temperature under nitrogen. Water and toluene are added to the reaction mixture and the mixture filtered. The filtrate is diluted with water, and the aqueous layer removed. The organic layer is washed with water (4×40 mL), and dried by azeotropic distillation. The solution is concentrated to give 1,2-dichloro-3-chloromethyl-4-nitrobenzene which could be used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06194420B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-ca2462a83f7c444d9419560a4855e476 |
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| Source note | uspto-grants-2001_02 |
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