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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416683Generated: October 30, 2026

Hydrogen Bromide → 1-Bromo-2,3-dichlorobenzene

https://huagongshe.com/reaction/416683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant2,3-DichloroanilineHCID 11844—
ReactantSodium BromideHCID 253881—
ReactantSodium NitriteHCID 23668193—
CatalystCopper SulfateHCID 24462—
SolventWaterHCID 962—
Product1-Bromo-2,3-dichlorobenzeneHCID 4206697.4%

Reaction Conditions

Temperature35 °C

Reaction Steps

32.7 g 2,3-Dichloroaniline (0.20 mole) is added to a mixture of 21.4 g of NaBr (0.20 mole, 1.0 equivalent), 110.0 g of 48% aqueous HBr (0.66 mole, 3.3 equivalents) and 70 ml water at 30-40° C. The mixture is stirred for 15 minutes at 30-40° C. and then heated to 45° C. Then 5.1 g CuSO4*5H2O (0.02 mole, 0.10 equivalent) is added and the mixture is stirred for 15 minutes at 45° C. After this, an aqueous solution of NaNO2 (40% solution in water, 37.6 g, 0.22 mole, 1.1 equivalents) is added via subsurface feeding over a period of 2 hours at 45° C. The reaction mixture is stirred for 30 minutes at 45° C. After this, the reaction mixture is heated to 60-65° C. The organic phase containing the reaction product is separated from the aqueous phase and is cooled to ambient temperature, leading to solidification of the reaction product. The remaining liquid is discarded and the crude product is washed twice with 10 ml water and dried under vacuum. 44.0 g (83% of theory) of 1-bromo-2,3-dichlorobenzene is obtained in the form of a light brown solid (purity: 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088960B2
Source datasetuspto-grants-2012_01
ORD IDord-1c7aad4968b64b30b17bf87a6d37f324
Source noteuspto-grants-2012_01