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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(1-Trityl-1H-imidazol-4-yl)propane-1,3-diol | HCID 21879607 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Hydroxy-1-(1-trityl-1H-imidazol-4-YL)propan-1-one | HCID 21879630 | 95.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07141598B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-21c82cd1b18945cbade7834660e31f83 |
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| Source note | uspto-grants-2006_11 |
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