HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl (3R)-3-morpholinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | (3R)-4-(tert-Butoxycarbonyl)morpholine-3-carboxylic acid | HCID 1512538 | — |
| Product | Methyl (3R)-3-morpholinecarboxylate | HCID 1514261 | — |
Reaction Steps
To a solution of (R)-morpholine-3,4-dicarboxylic acid-4-tert-butyl ester (5.00 g, 21.6 mmol) in MeOH (54 mL) was added thionyl chloride (3.16 mL, 43.2 mmol) dropwise, and the resulting mixture was heated at reflux for 16 h. The solution was cooled to ambient temperature and concentrated in vacuo. The residue was made basic with saturated aqueous NaHCO3 and extracted with CH2Cl2 (3×). The combined organic extracts were dried over Na2SO4, filtered, and concentrated in vacuo to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08765759B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-e1981ceb9301495aae7b28aed2065113 |
| Source note | uspto-grants-2014_07 |