HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → Ethyl (+/-)-4-(4-hydroxymethyl-1,3-oxazol-2-yl)-3-phenylbutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 11220404 | HCID 11220404 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl (+/-)-4-(4-hydroxymethyl-1,3-oxazol-2-yl)-3-phenylbutanoate | HCID 23389065 | 78% |
Reaction Steps
To a solution of ethyl (±)-4-(4-carboxy-1,3-oxazol-2-yl)-3-phenylbutanoate (500 mg, 1.65 mmole) in dry THF (8 mL) was added 4-methylmorpholine (0.22 mL, 1.99 mmole) then ethyl chloroformate (0.19 mL, 1.99 mmole) at 0° C. After 10 min, NaBH4 (249 mg, 6.59 mmole) was added all at once, then MeOH (8 mL) was added dropwise. After 30 min, the mixture was quenched with H2O (20 mL) and extracted with EtOAc (3×20 mL). The combined organic extracts were dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was chromatographed on silica gel (80% EtOAc/hexanes) to give the title compound (371 mg, 78%) as a yellow oil: MS (ES) m/e 290 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06458814B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-a10f23b0051d445689eb613a346e7c68 |
| Source note | uspto-grants-2002_10 |