HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → N-t-Butoxycarbonyl-2-Hydroxy-5-Chlorobenzylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Sulfate, hydrogen | HCID 61778 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | 2-(Aminomethyl)-4-chlorophenol | HCID 230844 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-t-Butoxycarbonyl-2-Hydroxy-5-Chlorobenzylamine | HCID 11311441 | — |
Reaction Steps
A mixture of 2-hydroxy-5-chlorobenzylamine (1.22 g, 4.77 mmol assuming the bisulfate salt), (BOC)2O (1.56 g, 7.16 mmol) and N-methylmorpholine (1.05 ml, 9.54 mmol) in DMF (10 ml) was stirred for 5 h at r.t. The reaction was partitioned between water and ethyl acetate and the organic layer was washed with 5% KHSO4 solution (2 times), sodium hydrogen carbonate solution and brine, dried (Na2SO4) and evaporated in vacuo to a solid. The crude product was recrystallized from ethyl acetate/hexanes (1:5, 12 ml) to give the title compound:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05792779 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-3abf86d272794b9ba786beb23e85acdd |
| Source note | uspto-grants-1998_08 |