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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077313Generated: October 30, 2026

Tetrahydrofuran → HCID 12319382, compound

https://huagongshe.com/reaction/1077313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 12213052HCID 12213052—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
ProductHCID 12319382HCID 12319382—

Reaction Steps

A solution of 8.5 g. of 1,3-dihydro-3-hydroxy-1'-methyl-3-phenylspiro[isobenzofuran-1,4'-piperidine], Example 1, in 150 ml. of tetrahydrofuran is added dropwise in 30 minutes to a stirred suspension of 2.0 g. of lithium aluminum hydride in 150 ml. of anhydrous tetrahydrofuran. The mixture is stirred at room temperature for 30 minutes and at 50° for 1 hour, cooled, diluted cautiously with water, and extracted with chloroform. The chloroform solution is dried over potassium carbonate and concentrated to a solid. Recrystallization from benzene gives colorless crystals, m.p. 190°-191° of 4-hydroxy-4-(α-hydroxy-α-phenyl-2-tolyl)-1-methylpiperidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03959475
Source datasetuspto-grants-1976_05
ORD IDord-ed58efbfc5844f6fbb16794934710938
Source noteuspto-grants-1976_05