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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077318Generated: November 4, 2026

Tetrahydrofuran → HCID 12213082, compound

https://huagongshe.com/reaction/1077318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1-Methyl-4-piperidoneHCID 74049—
ReactantHCID 12319472HCID 12319472—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
ProductHCID 12213082HCID 12213082—

Reaction Steps

To a cold (-60°) stirred solution of 2-bromobenzhydryl methyl ether in 38 ml. of tetrahydrofuran and 14 ml. of hexane is slowly added 53 ml. of 2.1 M n-butyllithium in hexane. After 2 hours, a solution of 10.7 g. of 1-methyl-4-piperidone in 15 ml. of tetrahydrofuran is added dropwise, and the suspension is stirred at -60° for 3 hours and at room temperature for 15 hours. Ice and water are added and the mixture is extracted with chloroform. The chloroform solution is dried over sodium sulfate and concentrated to a mixture of 4-hydroxy-4-(α-methoxy-α-phenyl-2-tolyl)-1-methylpiperidine and benzhydrol methyl ether. This oil is heated under reflux for 30 minutes if 240 ml. of acetic acid containing 60 ml. of hydrochloric acid. Dilution with water and addition of excess sodium hydroxide effects precipitation of a solid. Recrystallization from hexane provides 1,3-dihydro-1'-methyl-3-phenylspiro[isobenzofuran-1,4'-piperidine], m.p. 123°-124°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03959475
Source datasetuspto-grants-1976_05
ORD IDord-ab1021a9041f4ffca25bcf547a0e0cb0
Source noteuspto-grants-1976_05