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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063271Generated: October 31, 2026

Hydrochloric Acid → 1-Trityl-1H-imidazole-4-carboxylic acid

https://huagongshe.com/reaction/2063271

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
ReactantTrityl chlorideHCID 6456—
ReactantTriethylamineHCID 8471—
ReactantMethyl 1H-imidazole-5-carboxylateHCID 565661—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-Trityl-1H-imidazole-4-carboxylic acidHCID 10570117—

Reaction Steps

3H-Imidazole-4-carboxylic acid methyl ester (9.86 g, 78.2 mmol) is taken up in 150 mL DCM, triethylamine (11.9 mL, 86.0 mmol) is added and the reaction mixture is stirred for 5 min at RT. Chlorotriphenylmethane (24.0 g, 86.0 mmol) is added and the reaction mixture is stirred overnight at RT. The reaction mixture is extracted with an aqueous 5% NaHCO3 solution, the organic phase is dried over MgSO4 and concentrated under reduced pressure. The residue (20.7 g) is taken up in 100 mL MeOH, a solution of lithium hydroxide (4.80 g, 24.0 mmol) in 20 mL water is added drop wise and the reaction mixture is stirred over weekend at RT. The reaction mixture is acidified to pH 4 with 6N hydrochloric acid, 200 mL DCM is added and the two phase mixture is stirred vigorously. The phases are separated and the organic phase is dried over MgSO4 and concentrated under reduced pressure. Yield: 19.2 g. HPLC-MS: double peak tR=2.55/2.67 min, (M−H)−=353.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288379B2
Source datasetuspto-grants-2012_10
ORD IDord-ae7d40e5f3a74283aa13cd17a97c1e6b
Source noteuspto-grants-2012_10