HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → N-Benzylnormechlorethamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bis(2-chloroethyl)amine hydrochloride | HCID 522769 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-Benzylnormechlorethamine | HCID 5928 | — |
Reaction Steps
Using an ice bath, a mixture of 150 g of N,N-bis(2-chloroethyl)amine hydrochloride and 100 ml of benzyl bromide in 1000 ml of DMF is cooled and then 120 ml of triethylamine are added dropwise and the mixture is left overnight with stirring at AT. The reaction mixture is concentrated under vacuum, the residue is taken up with water and extracted 3 times with ether, the organic phases are dried over Na2SO4 and the solvent is evaporated under vacuum. This gives 113 g of the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07652011B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-a1e59e7587e643c0bebd7d0abbfbbe2f |
| Source note | uspto-grants-2010_01 |