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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580272Generated: November 3, 2026

Tetrahydrofuran → HCID 12251261, compound

https://huagongshe.com/reaction/1580272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 131709908HCID 131709908—
SolventWaterHCID 962—
ProductHCID 12251261HCID 1225126193%

Reaction Steps

A solution of 22.3 g. (0.77 M) of 4-benzyl-4-carbomethoxy-1-cyclohexaneone ethylene ketal [5] (prepared as in Example 4B) in 220 ml. of tetrahydrofuran is added to 3 g. of lithium aluminum hydride in 30 ml. of tetrahydrofuran. The mixture is stirred at reflux temperature for about 5.5 hours and then cooled in ice. There is added successively 3 ml. of water, 3 ml. of aqueous 15% sodium hydroxide solution and 9 ml. of water. The inorganic gel is collected on a filter and the filtrate evaporated to dryness. The residue is recrystallized from methylene chloride: Skellysolve B to give 18.8 g. (93% yield) of 4-benzyl-4-hydroxymethylcyclohexan-1-one ethylene ketal (1), having a melting point of 76° to 78° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03932425
Source datasetuspto-grants-1976_01
ORD IDord-9b6148131b1949d487c2569c3f8ef76b
Source noteuspto-grants-1976_01