HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890238Generated: October 31, 2026
2,3-Dichloronitrobenzene → HCID 12096330, compound
https://huagongshe.com/reaction/890238
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3-Dichloronitrobenzene | HCID 18555 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178456138 | HCID 178456138 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12096330 | HCID 12096330 | — |
Reaction Steps
1 600 ml of 0.5M isopropenylmagnesium bromide in THF are introduced under nitrogen and are cooled to −20° C., 51.2 g of 2,3-dichloronitrobenzene in 250 ml of anhydrous THF are added and the mixture is left stirring for I hour at −20° C. The reaction medium is poured at −20° C. onto 1 liter of saturated NH4Cl solution, the mixture is diluted with Et2O and then the aqueous phase is washed twice with Et2O. The organic phases are combined and are concentrated to dryness. The residue is extracted with DCM and the organic phase is washed twice with water and then with a saturated NaCl solution. It is dried and then evaporated and the residue is chromatographed on [lacuna] a hexane/AcOEt (95/5, v/v) mixture. 24.27 g of the expected compound are obtained, M.p.=70–71° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06995184B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-7a30ae80f6cc4854a9c90617f44f539f |
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| Source note | uspto-grants-2006_02 |
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