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 | US08198453B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-c44805062cf641a794ff581b4940c4c3 |
| Source note | uspto-grants-2012_06 |