HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 842580Generated: October 31, 2026
Diisopropylamine → Dichloro(diisopropylamino)borane
https://huagongshe.com/reaction/842580
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Boron Trichloride | HCID 25135 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Dichloro(diisopropylamino)borane | HCID 4139105 | 51% |
Reaction Steps
To a methylene chloride solution of trichloroborane (1.0 M, 100 ml, 0.10 mole) was added dropwise at −78° C. diisopropylamine (13.108 ml, 0.100 mole) over a 30 minute period. The solution was allowed to stir for 1 hour, during which a white precipitate formed. The mixture was allowed to warm to room temperature, and solvent was removed under reduced pressure. The residue was dissolved in 100 ml of dry toluene, triethylamine (13.94 ml, 0.10 mole) was added and the solution was stirred overnight at room temperature. The mixture was filtered, the residue was washed with 20 ml of toluene. Solvent was removed under reduced pressure from the combined filtrates, and the resulting oil was purified by vacuum distillation (25-28° C., 13 Pa, 0.1 mm) to give 9.2 g (51 percent) of product as a colorless liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06376406B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-b9b7822e9984409395c366ed641c0d1e |
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| Source note | uspto-grants-2002_04 |
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