HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-butyl 2-(methoxy(methyl)carbamoyl)morpholine-4-carboxylate → HCID 57449676, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-butyl 2-(methoxy(methyl)carbamoyl)morpholine-4-carboxylate | HCID 57449675 | — |
| Reactant | HCID 178495008 | HCID 178495008 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57449676 | HCID 57449676 | 93% |
Reaction Steps
A stirred solution of (±)-tert-butyl 2-(methoxy(methyl)carbamoyl)morpholine-4-carboxylate (1.73 g, 6.4 mmol) in dry THF (40 mL) was cooled in an ice-salt bath and 1.34 M 4-methoxybutylmagnesium chloride in THF (10 mL, 1.34 mmol) was added dropwise over 3 min. The cooling bath was allowed to expire and the mixture was stirred at rt for 6 h, poured into ice cold 3% aq HCl (100 mL) and extracted with ether (2×100 mL). The combined ether extracts were washed with satd aq NaHCO3 (35 mL), dried over MgSO4 and concentrated to afford (±)-tert-butyl 2-(5-methoxypentanoyl)morpholine-4-carboxylate (1.78 g, 93%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07754737B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-e6f728ee77034f0b901f0e96e8f9f4ac |
| Source note | uspto-grants-2010_07 |