HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657360Generated: October 30, 2026
3-Bromo-4-chlorobenzamide → 3-Bromo-4-chlorobenzylamine
https://huagongshe.com/reaction/657360
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Bromo-4-chlorobenzamide | HCID 53216663 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Bromo-4-chlorobenzylamine | HCID 57813392 | — |
Reaction Steps
To 3-bromo-4-chlorobenzamide (1.6 g, 6.8 mmol) in THF (10 mL) was added borane dimethyl sulfide complex (1.36 mL, 13.6 mmol) at room temperature. The mixture was then heated to 60° C. for 8 days. The solvent was pumped off and the reaction cautiously quenched with ethanol. When bubbling ceased, 1N HCl was added until the pH was ˜2. The mixture was stirred at 50° C. for 4 h. The mixture was partitioned between EtOAc and water. The aqueous phase was washed 3× with EtOAc. The aqueous phase was then adjusted to pH 10 with 2N NaOH and extracted 3× with EtOAc. The combined organics phases were washed with brine, dried over anhydrous Na2SO4, filtered, and evaporated to afford the title compound as a clear oil. LC-MS m/z 219.6 (M+H)+, 1.41 min (ret time).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071588B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-2111612c195645ad9d92bbf8fd1a5fc4 |
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| Source note | uspto-grants-2011_12 |
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