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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480448Generated: October 29, 2026

(6-tert-Butyldimethylsilyloxy-2-naphthyl)(1-trityl-1H-imidazol-4-yl)methanol → (6-tert-Butyldimethylsilyloxy-2-naphthyl)(1-trityl-1H-imidazol-4-yl)methanone

https://huagongshe.com/reaction/480448

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-tert-Butyldimethylsilyloxy-2-naphthyl)(1-trityl-1H-imidazol-4-yl)methanolHCID 18769033—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
Product(6-tert-Butyldimethylsilyloxy-2-naphthyl)(1-trityl-1H-imidazol-4-yl)methanoneHCID 1876905492.8%

Reaction Steps

To a solution of (6-tert-butyldimethylsilyloxy-2-naphthyl)(1-trityl-1H-imidazol-4-yl)methanol (49.0 g) in dichloromethane (400 mL) was added MnO2 (150 g) and the mixture was stirred for 3 h at room temperature. The reaction mixture was filtered and the filtrate was concentrated to give the titled compound (45.3 g) as a pale yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06649643B1
Source datasetuspto-grants-2003_11
ORD IDord-c75ad8a8dc244fe7a7ad4b21a5cf47ee
Source noteuspto-grants-2003_11