HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1046632Generated: October 31, 2026
2,6-Dichloroaniline → HCID 178512060, compound
https://huagongshe.com/reaction/1046632
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,6-Dichloroaniline | HCID 11846 | — |
| Reactant | 5-Bromothiophene-2-carbonitrile | HCID 3595059 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178512060 | HCID 178512060 | 103.2% |
Reaction Steps
To a stirred solution of 2,6-dichloroaniline (1.75 g, 10.8 mmol) in toluene (25 mL, anhyd) was added dropwise a 2.0M solution of trimethylaluminum in toluene (8.0 mL, 16 mmol). After 90 min the reaction mixture was charged with a solution of 5-bromothiophene-2-carbonitrile (3.00 g, 16 mmol) in toluene (20 mL, anhyd) and then heated at 90° C. After 5 h the reaction mixture was allowed to cool to ambient temperature and quenched by addition to a stirred slurry of silica (25 g) in 3:1 CHCl3/MeOH (100 mL). After 30 min the resulting mixture was filtered and the solids rinsed with MeOH and DCM. The combined filtrates were concentrated to afford the title compound (3.9 g, quant) as a pale yellow solid, which was used in the next step without purification. GC-MS (EI): 348, 350, 352.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569352B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-60f8b133d68242bba25cd3e019ee2f05 |
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| Source note | uspto-grants-2013_10 |
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