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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724207Generated: October 30, 2026

1-(1-Trityl-1H-imidazol-4-yl)propane-1,3-diol → 3-Hydroxy-1-(1-trityl-1H-imidazol-4-YL)propan-1-one

https://huagongshe.com/reaction/724207

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(1-Trityl-1H-imidazol-4-yl)propane-1,3-diolHCID 21879607—
CatalystHCID 178418406HCID 178418406—
SolventDichloromethaneHCID 6344—
Product3-Hydroxy-1-(1-trityl-1H-imidazol-4-YL)propan-1-oneHCID 2187963095.6%

Reaction Steps

1-(1-Trityl-1H-imidazol-4-yl)-1,3-propanediol (135.9 g) was dissolved in dichloromethane (1.76 L) and manganese dioxide (262 g) was added, which was followed by vigorous stirring at room temperature for 66 h. An insoluble material was filtered off by celite filtration and the filtrate was concentrated to dryness. The residue was suspended in ethyl acetate (1.5 L) and an aqueous solution (1 M; 3.5 L) of Rochelle salt was added, which was followed by stirring with a mechanical stirrer for 3 days. The reaction mixture was partitioned, and the organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. The aqueous layer was extracted again with ethyl acetate and treated in the same manner. The organic layer was combined and the solvent was evaporated to give the title compound (129.3 g) as a pale-brown caramel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141598B2
Source datasetuspto-grants-2006_11
ORD IDord-21c82cd1b18945cbade7834660e31f83
Source noteuspto-grants-2006_11