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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486431Generated: October 31, 2026

Toluene → HCID 67823394, compound

https://huagongshe.com/reaction/486431

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPhenylacetonitrileHCID 8794—
ReactantSodium amideHCID 24533—
ReactantEthyl 1-benzylpiperidine-4-carboxylateHCID 90423—
SolventBenzeneHCID 241—
SolventEthanolHCID 702—
ProductHCID 67823394HCID 6782339438%

Reaction Conditions

Temperature30 °C

Reaction Steps

To a stirred mixture of 7.8 parts of sodium amide 5% in benzene and 135 parts of methylbenzene was added dropwise a solution of 11.7 parts of benzeneacetonitrile in 45 parts of methylbenzene at 25° C (cooling was necessary). After stirring for 30 minutes at 30° C., there was added dropwise a solution of 24.7 parts of ethyl 1-(phenylmethyl)-4-piperidinecarboxylate in 45 parts of methylbenzene at 30° C. Upon completion, stirring was continued overnight at 80° C. The reaction mixture was cooled, 12 parts of ethanol were added and the whole was poured into ice water. The layers were separated and the aqueous phase was neutralized with acetic acid The oily Product was extracted with trichloromethane. The extract was dried, filtered and evaporated. The residue was crystallized from 4-methyl-2-pentanone, yielding 12 parts (38%) of α-[hydroxy[1-(phenylmethyl)-4-piperidinyl]methylidene]-benzeneacetonitrile: mp. 191.9° C. (intermediate 5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292738
Source datasetuspto-grants-1994_03
ORD IDord-48267bd9a3234dfa88f4c2ae9a78898f
Source noteuspto-grants-1994_03