HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Tert-butyl 3-(benzylamino)-3-(2-fluorobenzyl)cyclohexylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Tert-butyl 3-(benzylimino)cyclohexylcarbamate | HCID 67983484 | — |
| Reactant | HCID 178505627 | HCID 178505627 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 3-(benzylamino)-3-(2-fluorobenzyl)cyclohexylcarbamate | HCID 67983661 | — |
Reaction Steps
To the solution of tert-butyl 3-(benzylimino)cyclohexylcarbamate (4 mmol) in THF (10 mL) was added a solution of (2-fluorobenzyl)magnesium chloride in ether (9 mmol, 0.25 M, 36 mL) at 0° C. The reaction mixture was allowed to warm to room temperature and stirred for overnight. The reaction mixture was added to the iced water. The organics were extracted using EtOAc from the aqueous mixture. The EtOAc solution was concentrated. The product, tert-butyl 3-(benzylamino)-3-(2-fluorobenzyl)cyclohexylcarbamate, was purified by column chromatography on silica gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09351965B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-ee52f911baa84fcf90879aae4e6c04ec |
| Source note | uspto-grants-2016_05 |