Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 4-chloroacetoacetate | HCID 69484 | — |
| Reactant | 2-(2,4,5-Trimethyl-1H-imidazol-1-yl)ethan-1-ol | HCID 21283688 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13457163 | HCID 13457163 | 37% |
Reaction Steps
Sodium hydride (80% dispersion in oil) (7.8 g) was suspended in dry tetrahydrofuran (100 ml). 2-(2,4,5-Trimethylimidazol-1-yl)ethanol (20 g) was added and the suspension sonicated until there was no further gas evolution. Ethyl 4-chloroacetoacetate (21.3 g) in dry tetrahydrofuran (25 ml) was added over 0.75 hours with sonication, and sonication continued for a further 4 hours. The suspension was poured into 2N hydrochloric acid (200 ml) and the tetrahydrofuran removed under vacuum. The aqueous solution was washed with dichloromethane (3×50 ml) and then neutralised with potassium carbonate. The aqueous phase was extracted with dichloromethane (5×100 ml), the combined organic extracts dried over magnesium sulphate and solvent removed under vacuum. The crude product was chromatographed over silica eluting with a mixture of methanol and ethyl acetate (1:3) to yield the title compound as a pale red oil 13.5 g (37%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04788205 |
|---|
| Source dataset | uspto-grants-1988_11 |
|---|
| ORD ID | ord-2a764efc0d494d2d90fe3ffad7733ede |
|---|
| Source note | uspto-grants-1988_11 |
|---|