HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604429Generated: October 31, 2026
HCID 22456838, compound → HCID 22456853, compound
https://huagongshe.com/reaction/1604429
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 22456838 | HCID 22456838 | — |
| Reactant | HCID 178506676 | HCID 178506676 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22456853 | HCID 22456853 | 3% |
Reaction Steps
A solution of (±)-1-[2-(3,4-dimethoxyphenyl)-2-ethoxyethyl]-1,3-dihydro-3-(phenylmethyl)-2H-imidazol-2-one (4.86 g) in THF (100 ml) was stirred at RT. Phenyllithium (1.278 g) was added dropwise and the mixture was stirred overnight at RT. The mixture was carefully poured out into ice/water (200 ml), then extracted three times with CH2Cl2 (150 ml). The separated organic layer was dried (MgSO4), filtered, and the solvent was evaporated The residue was purified by short column chromatography over silica gel (eluent: CH2Cl2 /(CH3OH/NH3) 95/5). The desired fractions were collected and the solvent was evaporated. The residue was crystallized from ethylacetate. The precipitate was filtered off, wased with ethylacetate and DIPE, then dried, yielding 0.1 g (3%) of (±)-1-[2(3,4-dimethoxyphenyl)-2-ethoxyethyl]-1,3-dihydro-2H-imidazol-2-one (comp. 15; mp. 133.6° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05994376 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-9dac0b8badc2404ba98505cd2a0c5791 |
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| Source note | uspto-grants-1999_11 |
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