HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → (R)-benzyl 1-hydroxy-3-(2-oxopyrrolidin-1-yl)propan-2-ylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (R)-benzyl 1-(4-chlorobutanamido)-3-hydroxypropan-2-ylcarbamate | HCID 86639450 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (R)-benzyl 1-hydroxy-3-(2-oxopyrrolidin-1-yl)propan-2-ylcarbamate | HCID 59201635 | 33% |
Reaction Steps
A solution of (R)-benzyl 1-(4-chlorobutanamido)-3-hydroxypropan-2-ylcarbamate (3.9 g, 11.9 mmol) in DMF was cooled to 0° C., followed by the addition of NaH (0.72 g, 17.9 mmol). The mixture was stirred at rt for 4 h. DMF was removed under high vacuum, and the residue was taken up in EtOAc, washed with 1 N HCl, saturated NaHCO3, NaCl, dried over Na2SO4, and concentrated to give the crude product, which was purified by column chromatography to give (R)-benzyl 1-hydroxy-3-(2-oxopyrrolidin-1-yl)propan-2-ylcarbamate (1.1 g, yield 33%). 1H NMR (CDCl3, 400 MHz) δ 7.39-7.27 (m, 5H), 5.45 (d, 1H), 5.10 (d, 1H), 4.70 (s, 2H), 3.72 (m, 1H), 3.54-3.40 (m, 4H), 3.20-3.17 (m, 1H), 2.40 (t, 2H), 2.07 (t, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08487108B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-8961601b2182411292807a2e54076422 |
| Source note | uspto-grants-2013_07 |