HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → (1-Trityl-1H-imidazol-4-yl)acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | HCID 178479752 | HCID 178479752 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (1-Trityl-1H-imidazol-4-yl)acetic acid | HCID 11090087 | — |
Reaction Steps
Trityl chloride (51 g, 0.18 mol) is added to a suspension of (1H-imidazol-4-yl)acetic acid hydrochloride (25 g, 0.15 mol) in pyridine (500 mL). This is stirred at room temperature for 16 h, at the end of which MeOH (150 mL) is added. This solution is stirred at room temperature for 1 h. Solvents are evaporated and the residue is taken up in CH2Cl2 and washed with 1 M aqueous citric acid solution (2×) and brine. The organic phase is dried over anhydrous Na2SO4 and evaporated to give a sticky residue which when taken up in diethyl ether and evaporated gave the product as a white solid that is used without further purification. MS (ESI) m/z 368.9 (M+H) (Procedure adapted from J. Org. Chem. 1993, 58, 4606, also prepared in WO2003013526)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08835646B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-a53f227d0aa2401cb60c378457e91a42 |
| Source note | uspto-grants-2014_09 |