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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2076008Generated: October 27, 2026

Bromine → [3-Bromo-1-(4-chloro-phenyl)-2-oxo-cyclohexyl]-acetonitrile

https://huagongshe.com/reaction/2076008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant[1-(4-Chlorophenyl)-2-oxo-cyclohexyl]-acetonitrileHCID 68911510—
SolventChloroformHCID 6212—
Product[3-Bromo-1-(4-chloro-phenyl)-2-oxo-cyclohexyl]-acetonitrileHCID 6709612679.6%

Reaction Conditions

Temperature5 °C

Reaction Steps

1-(4-Chloro-phenyl)-2-oxo-cyclohexyl-acetonitrile (100 mg, 0.40 mmol) was dissolved in chloroform (1 mL). To this solution bromine (67.7 mg, 0.42 mmol) in chloroform (0.5 mL) was added drop wise at −11° C. The reaction was stirred for 1½ hours at 5° C., then for 1 hours t room temperature and finally for 1 hour at 50° C. The solvent was removed under reduced pressure and the residue was purified by column chromatography on silica gel using dichloromethane as eluent to yield the title compound (104 mg, 79%) as colourless oil. NMR (CDCl3, 300 MHz): δ (ppm)=7.44 (d, 2H), 7.13 (d, 2H), 4.62 (dd, 1H), 2.99 (m, 2.80 (s, 2H), 2.58 (m, 1H), 2.14 (m, 1H), 1.92 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923450B2
Source datasetuspto-grants-2011_04
ORD IDord-5a19e041e9f2485f8dd1062e8d0c5cc3
Source noteuspto-grants-2011_04