HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19789Generated: October 30, 2026
1,3-Dibromo-5-chlorobenzene → 1-Bromo-3-chloro-5-cyclopropylbenzene
https://huagongshe.com/reaction/19789
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Dibromo-5-chlorobenzene | HCID 84676 | — |
| Reactant | HCID 178418630 | HCID 178418630 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-Bromo-3-chloro-5-cyclopropylbenzene | HCID 66520960 | 64% |
Reaction Steps
To a solution of 1,3-dibromo-5-chlorobenzene (500 mg, 1.85 mmol) in THF (1 ml) was added cyclopropylmagnesium bromide (3698 μl, 0.5M solution in THF, 1.85 mmol) in a sealed tube and the reaction mixture was degassed with argon for 5 min before tetrakis(triphenylphosphine)palladium (0) (107 mg, 0.09 mmol) was added. The resulting solution was heated to 70° C. overnight, cooled to RT and then quenched with sat. NH4Cl solution and extracted with pentane. The organic phases were combined, washed with water and brine, dried over MgSO4 and filtered through a short pad of silica gel to give the desired product (272 mg, 64%) which did not require further purification. 1H NMR (CDCl3, 300 MHz): 7.28 (aptt, J=2.0 Hz, 1H), 7.08 (aptt, J=1.5 Hz, 1H), 6.97 (aptt, J=1.5 Hz, 1H), 1.83 (m, 1H), 1.04-0.97 (m, 2H), 0.72-0.67 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07745477B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-2b7debaa34934d1abbc3bc7f4dd483ae |
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| Source note | uspto-grants-2010_06 |
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