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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923242Generated: November 2, 2026

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

https://huagongshe.com/reaction/923242

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 numberUS09278969B2
Source datasetuspto-grants-2016_03
ORD IDord-2d601936c61145f2a6f139ce6179ef3e
Source noteuspto-grants-2016_03