HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → D-1-N-Boc-prolinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | (2R)-1-[(tert-butoxy)carbonyl]pyrrolidine-2-carboxylic acid | HCID 688022 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | D-1-N-Boc-prolinamide | HCID 2756826 | 54.3% |
Reaction Steps
N-Methylmorpholine (9.85 g, 97.5 mmol) and isobutyl chloroformate (13.33 g, 97.5 mmol) was added to (R)-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester (20.0 g, 92.9 mmol) in THF (200 mL) at −78° C. and stirred for 1 h. Ammonium hydroxide (58 mL) was added slowly as the reaction warmed up to RT and stirred for a further 2 h. The reaction mixture was partitioned between DCM and water. The organic extracts were washed with 1 M HCl, dried over sodium sulphate, filtered and concentrated to afford the title product (10.8 g, 54%) as a colourless semisolid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07678796B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-14bc45ad321e40aeaecc5f402cf297d9 |
| Source note | uspto-grants-2010_03 |