HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398254Generated: October 30, 2026
Dibenzylamine → N,N-dibenzyl-3-chloropropan-1-amine
https://huagongshe.com/reaction/398254
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dibenzylamine | HCID 7656 | — |
| Reactant | 1-Bromo-3-chloropropane | HCID 8006 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Cyclohexane | HCID 8078 | — |
| Product | N,N-dibenzyl-3-chloropropan-1-amine | HCID 18482 | 53% |
Reaction Steps
To a stirred suspension of K2CO3 (200 g, 1.5 mole) in cyclohexane 200 mL and 1-bromo-3-chloropropane (540 gms, 3.4 mole) is added dropwise over a period of 1 h at 20° C. dibenzyl amine (442 g, 2.24 mole). After complete addition the reaction is allowed to stir for an additional 20 h. The crude reaction mixture is filtered and then washed with saturated NaCl (3×100 mL). The organic phase is extracted with 3N HCl (3×100 mL). The resulting aqueous phase, containing the desired product as the hydrochloric salt, is washed with hexanes (3×100 mL) to remove any residual BCP. The aqueous phase is subsequently basified with 50wt % NaOH and extracted with cyclohexane (3×100 mL). After solvent removal 324 g (53% yield) of the title compound was isolated as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610859B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-d1b0af979cd542229f0e9c318262ebc5 |
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| Source note | uspto-grants-2003_08 |
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