HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → (9H-fluoren-9-yl)methyl 4-(bromoacetyl)piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 9H-fluoren-9-ylmethyl-4-(diazoacetyl)piperidine-1-carboxylate | HCID 86647449 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (9H-fluoren-9-yl)methyl 4-(bromoacetyl)piperidine-1-carboxylate | HCID 86685241 | 53% |
Reaction Steps
A solution of (9H-fluoren-9-yl)methyl 4-(diazoacetyl)piperidine-1-carboxylate (5 g, 13.3 mmol) in THF was cooled in an ice water bath and was treated with an aqueous HBr solution (10 mL). This reaction mixture was stirred at RT for 2 h. The reaction mixture was diluted with water and the organic content was extracted using EtOAc, dried over Na2SO4, filtered and concentrated at reduced pressure. The crude product was chromatographed over silica gel eluting with a gradient (0-15% EtOAc:hexanes) to afford (9H-fluoren-9-yl)methyl 4-(bromoacetyl)piperidine-1-carboxylate (3 g, 53%) as an off white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09334269B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-df99140cba08482bb3c56295135abb14 |
| Source note | uspto-grants-2016_05 |