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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 76861Generated: October 30, 2026

Methanol → (1-Trityl-1H-imidazol-4-yl)acetic acid

https://huagongshe.com/reaction/76861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTrityl chlorideHCID 6456—
ReactantHCID 178479752HCID 178479752—
SolventPyridineHCID 1049—
SolventDiethyl EtherHCID 3283—
Product(1-Trityl-1H-imidazol-4-yl)acetic acidHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835646B2
Source datasetuspto-grants-2014_09
ORD IDord-a53f227d0aa2401cb60c378457e91a42
Source noteuspto-grants-2014_09