HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499737Generated: October 31, 2026
Dimethylformamide → 2-Bromo-6-chloro-4-(1-chloroethyl)-3-ethoxybenzonitrile
https://huagongshe.com/reaction/1499737
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | 2-Bromo-6-chloro-3-ethoxy-4-(1-hydroxyethyl)benzonitrile | HCID 86677666 | — |
| Product | 2-Bromo-6-chloro-4-(1-chloroethyl)-3-ethoxybenzonitrile | HCID 86677667 | 75.8% |
Reaction Steps
Cyanuric chloride (0.11 g, 0.59 mmol) was dissolved in N,N-dimethylformamide (3 mL, 40 mmol). After stirring for a few minutes, a solution of 2-bromo-6-chloro-3-ethoxy-4-(1-hydroxyethyl)benzonitrile (150 mg, 0.49 mmol) in methylene chloride (3 mL, 50 mmol) was added. The resulting mixture was stirred at room temperature overnight. The reaction was partitioned between water and dichloromethane. The organic layer was washed with sat. NaHCO3 solution, water, brine, dried over MgSO4, and concentrated. The crude product was purified by flash column chromatography, eluting a gradient of 0-30% EtOAc/Hexane to give 2-bromo-6-chloro-4-(1-chloroethyl)-3-ethoxybenzonitrile (0.12 gm, 75%) as a semisolid, LCMS calculated for C11H10BrCl2NO m/z=323.9, 320.9; found: (poor ionization).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09199982B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-2cfc2100b04a4906aac43b8cb25f2f0b |
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| Source note | uspto-grants-2015_12 |
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