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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | [1-(4-Chlorophenyl)-2-oxo-cyclohexyl]-acetonitrile | HCID 68911510 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | [3-Bromo-1-(4-chloro-phenyl)-2-oxo-cyclohexyl]-acetonitrile | HCID 67096126 | 79.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07923450B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-5a19e041e9f2485f8dd1062e8d0c5cc3 |
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| Source note | uspto-grants-2011_04 |
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