HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265970Generated: November 3, 2026
Hydrochloric Acid → 2-Bromo-3-(4-chlorophenyl)-1-propene
https://huagongshe.com/reaction/1265970
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,3-Dibromopropene | HCID 10552 | — |
| Reactant | HCID 178478191 | HCID 178478191 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Bromo-3-(4-chlorophenyl)-1-propene | HCID 10036892 | 83.6% |
Reaction Steps
A solution of 8 ml (0.0622 mol) of 2,3-dibromopropene in 50 ml diethyl ether was placed under a nitrogen atmosphere by use of a Firestone valve. While cooling in an ice water bath, a solution of 62 ml (0.062 mol) of 1M 4-chlorophenylmagnesium bromide in diethyl ether was added slowly via addition funnel. After stirring for 2 hours while warming to room temperature, the reaction was recooled in an ice bath and 50 ml of 1 N hydrochloric acid was then added via syringe. The resulting mixture was transferred to a separatory funnel and the phases were separated. The organic layer was dried over MgSO4 and filtered. The solvent was removed from the filtrate in vacuo. The residue was triturated with cold pentanes to yield 12.0 g of 1-(2-bromo-allyl)-4-chloro-benzene as an oil which was used in without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06548448B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-879948f9dd66455ca47f51561b47d8bf |
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| Source note | uspto-grants-2003_04 |
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