HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Methoxymethyl)-1,3-dioxolan-2-one → t-butyl (RS)-4-[4-(5-methoxymethyl-2-oxo-oxazolidin-3-yl)-phenyl]-piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Methoxymethyl)-1,3-dioxolan-2-one | HCID 4384485 | — |
| Reactant | t-Butyl 4-(4-ethoxycarbonylamino-phenyl)-piperidine-1-carboxylate | HCID 23371871 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | t-butyl (RS)-4-[4-(5-methoxymethyl-2-oxo-oxazolidin-3-yl)-phenyl]-piperidine-1-carboxylate | HCID 86749979 | 58% |
Reaction Steps
5.5 g (15.0 mmol) of t-butyl 4-(4-ethoxycarbonylamino-phenyl)-piperidine-1-carboxylate and 20 g (0.15 mol) of (RS)-4-(methoxymethyl)-1,3-dioxolan-2-one were stirred intensively in the presence of 2.37 g of pyridine for 18 hours at an oil bath temperature of 160°. After cooling the reaction mixture it was chromatographed on 840 g of silica gel 60 with ether. 3.4 g of t-butyl (RS)-4-[4-(5-methoxymethyl-2-oxo-oxazolidin-3-yl)-phenyl]-piperidine-1-carboxylate were obtained as a yellowish oil. 1H-NMR (CDCl3) ppm: 7.48 (d,2H), 7.22 (d,2H), 4.76 (m,1H), 4.25 (bd,2H), 4.05 (t,1H), 3.92 (t,1H), 3.64 (d,2H), 3.43 (s,3H), 2.80 (t,2H), 2.64 (m,1H), 1.78 (bd,2H), 1.61 (m,2H), 1.49 (s,9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05574055 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-a6479b7751ff406e8cfc11632c7cbe18 |
| Source note | uspto-grants-1996_11 |