Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dibromo-5-chlorobenzeneHCID 84676—
ReactantHCID 178418630HCID 178418630—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product1-Bromo-3-chloro-5-cyclopropylbenzeneHCID 6652096064%

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745477B2
Source datasetuspto-grants-2010_06
ORD IDord-2b7debaa34934d1abbc3bc7f4dd483ae
Source noteuspto-grants-2010_06