Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Ethyl 2-(2,5,6-trimethylbenzimidazol-1-yl)acetate | HCID 21276952 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21276959 | HCID 21276959 | 37% |
Reaction Steps
A solution of ethyl 2-(2,5,6-trimethylbenzimidazol-1-yl)acetate (6.15 g) in dry tetrahydrofuran (20 ml) was added to a suspension of lithium aluminium hydride (0.95 g) was dry tetrahydrofuran (60 ml) at 0° C. The reaction was allowed to warm to room temperature and stirred at room temperature for 1 hour. Water (1 ml) was added dropwise to the reaction followed by 15% sodium hydroxide (3 ml) and water (3 ml). The suspension was filtered and the solvent removed under reduced pressure. The product was dissolved in dichloromethane, dried over magnesium sulphate and the solvent removed under reduced pressure. The residue was triturated with acetone, the solid filtered and dried under reduced pressure to yield the title compound (1.9 g, 37%), m.p. 191°-2° C. Found: C, 70.17; H, 8.07; N, 13.56. C12H16N2O requires: C, 70.59; H, 7.84; N, 13.72%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04801598 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-b2f1dec1082e48969d4a4f42904a5f6f |
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| Source note | uspto-grants-1989_01 |
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