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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416162Generated: October 27, 2026

Imidazole → 9-Methoxymethyl-9-[(tert-butyldimethylsilyl)oxymethyl]-fluorene

https://huagongshe.com/reaction/2416162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant9-(Methoxymethyl)-9H-fluorene-9-methanolHCID 22639103—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product9-Methoxymethyl-9-[(tert-butyldimethylsilyl)oxymethyl]-fluoreneHCID 2263912587.6%

Reaction Steps

1 g of 9-methoxymethyl-9-hydroxymethyl-fluorene (4.2 mmol) was dissolved in 10 ml of N,N-dimethyl formamide, and 0.14 g of imidazole was added thereto. The mixture was cooled in ice-water bath, and 0.87 ml of triethyl amine (6.2 mmol) was added thereto. After stirring for 5 minutes, 0.88 g of tert-butyldimethylsilyl chloride (5.8 mmol) in 10 ml of N,N-dimethyl formamide was added drop-wise, and the mixture was stirred for further 2 hours, followed by stirring at room temperature for 1 hour. The reaction mixture was diluted with 10 ml of water, and extracted twice using 20 ml of dichloromethane for each time. The combined dichloromethane extract was dried over anhydrous sodium sulfate. After filtration, the filtrate was evaporated to give 1.28 g of concentrate (yield 87.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06822109B2
Source datasetuspto-grants-2004_11
ORD IDord-f0e4dcd6c2f1423f8e9527c7f923011d
Source noteuspto-grants-2004_11