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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756426Generated: October 28, 2026

Tetrahydrofuran → HCID 53814882, compound

https://huagongshe.com/reaction/1756426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant2-(1-Adamantyl)-5-bromophenolHCID 22347853—
ProductHCID 53814882HCID 53814882—

Reaction Steps

1.6 g (53 mmol) of sodium hydride (80% in oil) and 50 mi of THF are introduced into a round-bottomed flask and a solution of 15 g (49 mmol) of the phenol obtained above in (a), dissolved in 100 mi of DMF, is added dropwise. The mixture is stirred until gaseous evolution has ceased and 3.1 ml (49 mmol) of methyl iodide are then introduced. The mixture is stirred at room temperature for four hours, the reaction medium is poured into water and the organic phase is separated after settling has taken place, then dried over magnesium sulphate and evaporated. The residue obtained is ground in the minimum amount of hexane and filtered off. 12.6 g (80%) of 2-(1-adamantyl)-5-bromoanisole, melting point 159°-160° C., are collected.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05439925
Source datasetuspto-grants-1995_08
ORD IDord-485b2132f278430293a9ab91a5dbd2f9
Source noteuspto-grants-1995_08