HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → Benzyl(2,2-difluoroethyl)amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chlorodifluoroethane (mixed isomers) | HCID 2736499 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzyl(2,2-difluoroethyl)amine | HCID 50896648 | 66% |
Reaction Steps
An amount of 10 g (92 mmol) of 2,2-difluoro-1-chloroethane, 5 g (46 mmol) of benzylamine and 5.2 g (51 mmol) of triethylamine are heated in 20 g of water in an autoclave at an internal temperature of 120° C. for 6 hours. The two-phase solution is twice extracted with 50 ml of dichloromethane each time and the combined organic phases are washed with 50 ml of water and subsequently distilled. An amount of 5.2 g of N-benzyl-2,2-difluoroethanamine is obtained, which corresponds to a yield of 66%, based on benzylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08450528B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-cb10cf0ca6834f6592604232eca3bfec |
| Source note | uspto-grants-2013_05 |