Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Phosphoric Acid | HCID 1004 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 68486336 | HCID 68486336 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68486406 | HCID 68486406 | 99.7% |
Reaction Steps
Lithium hydroxide (2 mL, 2 mmol, 1 M in H2O) was added to a solution of ethyl 4-methyl-2-(1-methylethyl)-1-({[2-(trimethylsilyl)ethyl]oxy}methyl)-1H-imidazole-5-carboxylate (133 mg, 0.41 mmol) in THF:MeOH (6 mL/2 mL). The reaction mixture was heated at 40° C. and stirred overnight. The mixture was then acidified by H3PO4 (1N), extracted with 10% MeOH in CHCl3 and the organic layer was dried over sodium sulfate. The solvent was evaporated and dried in vacuo to give the title compound (122 mg, >99%) as a yellow gel which was directly used in the next step without purification. LCMS: m/z 299 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304419B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-d58be7624307484080679492ac3d9268 |
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| Source note | uspto-grants-2012_11 |
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