HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 11163547, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzyl [(3R)-2,5-dioxopyrrolidin-3-yl]carbamate | HCID 44459755 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11163547 | HCID 11163547 | 74% |
Reaction Steps
1.2.2 (via two steps; 2nd step): A suspension of 48.4 mg of 60% NaH in 3 ml of THF was treated with 300 mg of (R)-(2,5-dioxo-pyrrolidin-3-yl)-carbamic acid benzyl ester at 0° C. followed by 161.3 μL of benzyl bromide. After 30 min the resulting precipitate was warmed to rt and treated with 3 ml of DMF to give after 15 min a solution which was stirred for 16 h at rt then quenched with 60 ml of H2O and extracted with 40 ml of toluene. The combined organic layers were dried over MgSO4 and concentrated to give 409 mg (74%) of the (R)-(2,5-dioxo-pyrrolidin-3-yl)-carbamic acid benzyl ester as white crystals; m.p. 145.1-145.5° C. Overall yield for the two step process: 78%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07262307B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-bddbd23d2478409189c542bd18376f23 |
| Source note | uspto-grants-2007_08 |