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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416159Generated: October 25, 2026

Methyl iodide → 9-(Methoxymethyl)-9H-fluorene-9-methanol

https://huagongshe.com/reaction/2416159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant9H-Fluorene-9,9-dimethanolHCID 345022—
SolventTetrahydrofuranHCID 8028—
Product9-(Methoxymethyl)-9H-fluorene-9-methanolHCID 2263910362%

Reaction Steps

Under nitrogen atmosphere and anhydrous condition, to a reactor were added in succession 80 ml of tetrahydrofuran, 22.6 g (0.1 mol) of 9,9-bis(hydroxymethyl)fluorene and 57 g (0.4 mol) of iodomethane. After the reaction mixture was admixed homogeneously by stirring, 4.6 g of 52% NaH in mineral oil (0.1 mol) was added batch-wise over 2 hours at room temperature, Upon completing the addition, the reaction mixture was stirred for further 2 hours. The unreacted iodomethane was recovered by distillation. The remainder was diluted with 100 ml of water, and extracted twice using 100 ml of diethyl ether for each time. The combined diethyl ether extract was dried over anhydrous sodium sulfate. After drying, thee ether solution was evaporated to dry to give 22.8 g of crude. The crude was purified through column chromatography to give 14.9 g of 9-methoxymethyl-9-hydroxymethyl-fluorene (yield 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06822109B2
Source datasetuspto-grants-2004_11
ORD IDord-d62ed08e665f431d83347205370dea20
Source noteuspto-grants-2004_11