HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylbenzylamine → 2,2-difluoro-N-(4-methylbenzyl)ethanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylbenzylamine | HCID 66035 | — |
| Reactant | Chlorodifluoroethane (mixed isomers) | HCID 2736499 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,2-difluoro-N-(4-methylbenzyl)ethanamine | HCID 60923068 | 58% |
Reaction Steps
An amount of 26.2 g (242 mmol) of 2,2-difluoro-1-chloroethane and 10 g of 4-methylbenzylamine (80.8 mmol) are heated in an autoclave at an internal temperature of 120° C. for 16 hours. Subsequently, 50 g of water are added and the aqueous phase is separated. The aqueous phase is again extracted with 2,2-difluoro-1-chloroethane and the combined organic phases are distilled as described in Example 1.1. Here also, the 4-methylbenzylamine hydrochloride which is present in the aqueous phase can be converted back into free 4-methylbenzylamine by addition of sodium hydroxide solution. After distillation, 4.3 g of 2,2-difluoro-N-(4-methylbenzyl)ethanamine are obtained, which corresponds to a yield of 58%, based on reacted 4-methylbenzylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08450528B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-a9015e25fd45480f8288826f21702d51 |
| Source note | uspto-grants-2013_05 |