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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 9-(Methoxymethyl)-9H-fluorene-9-methanol | HCID 22639103 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 9-Methoxymethyl-9-[(tert-butyldimethylsilyl)oxymethyl]-fluorene | HCID 22639125 | 87.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06822109B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-f0e4dcd6c2f1423f8e9527c7f923011d |
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| Source note | uspto-grants-2004_11 |
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