HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methoxypropene → Methyl (S)-3-Boc-2,2-dimethyloxazolidine-4-propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methoxypropene | HCID 8300 | — |
| Reactant | (S)-methyl 4-(tert-butoxycarbonylamino)-5-hydroxypentanoate | HCID 11107667 | — |
| Catalyst | Boron trifluoride etherate | HCID 8000 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl (S)-3-Boc-2,2-dimethyloxazolidine-4-propanoate | HCID 15930243 | 90% |
Reaction Steps
(S)-methyl 4-(tert-butoxycarbonylamino)-5-hydroxypentanoate (24 g, 97.2 mmol) and isopropenyl methyl ether (88.8 g, 854.6 mmol) was dissolved in acetone (2000 mL) and BF3.Et2O (0.82 mL, 5.84 mmol) was added at rt. The mixture was stirred for 1 hr at rt. The reaction was quenched by addition of Et3N (11.6 mL). The reaction solution was washed with aqueous saturated NaHCO3 (200 mL) and evaporated, and (S)-tert-butyl 4-(3-methoxy-3-oxopropyl)-2,2-dimethyloxazolidine-3-carboxylate (25.1 g, 90%) was obtained as an oil, which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08580823B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-528caa24af7645f0b5fe280b789415a4 |
| Source note | uspto-grants-2013_11 |