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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1077322Generated: October 31, 2026

Hydrochloric Acid → 3-Phenyl-3H-spiro[2-benzofuran-1,4'-piperidine]

https://huagongshe.com/reaction/1077322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 86733482HCID 86733482—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-Phenyl-3H-spiro[2-benzofuran-1,4'-piperidine]HCID 191510—

Reaction Steps

A mixture of 2.9 G. of 1'-benzyl-1,3-dihydro-3-phenylspiro[phenylspiro[isobenzofuran-1,4'-piperidine], (Example 4), 0.4 g. of 10% palladium on carbon, 20 ml. of 95% ethanol, and 2 ml. of conc. hydrochloric acid is hydrogenated at 50 p.s.i. and 50°. After hydrogen uptake ceases, the mixture is filtered and the filtrate concentrated. Recrystallization of the residue from cyclohexane provides colorless crystals, m.p. 119°-123°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03959475
Source datasetuspto-grants-1976_05
ORD IDord-9c2f915bdfe7497d8e74b2e39d611e7b
Source noteuspto-grants-1976_05