Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Imidazolidinone | HCID 8453 | — |
| Reactant | Bromoacetonitrile | HCID 11534 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20669979 | HCID 20669979 | 6% |
Reaction Steps
A solution of imidazolidin-2-one (0.75 g, 8.71 mmol) in DMF (17 mL) was treated drop-wise with LiHMDS (1M THF, 10.45 mL, 10.45 mmol), stirred for 2 h, treated with bromoacetonitrile (0.607 mL, 8.71 mmol) and heated at 45° C. overnight. The mixture was cooled to RT, treated with satd. NH4Cl, extracted with EtOAc (4×) and the combined organics were washed with brine, dried over Na2SO4, concentrated to dryness and purified via silica gel chromatography (MeOH/DCM) to afford 2-(2-oxoimidazolidin-1-yl)acetonitrile (65 mg, 6%). 1H NMR (400 MHz, DMSO-d6): δ 6.38 (s, 1 H), 4.66 (s, 2 H), 3.98-3.93 (m, 2H), 3.91-3.86 (m, 2H); MS (ESI) m/z: 126.1 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09133183B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-484303ba076f4eb79ded8c3e8990de87 |
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| Source note | uspto-grants-2015_09 |
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