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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486277Generated: October 29, 2026

2,6-Diphenylpiperidine → 1,4-Bis(2,6-diphenylpiperidin-1-yl)-2-butene

https://huagongshe.com/reaction/486277

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-DiphenylpiperidineHCID 13010638—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product1,4-Bis(2,6-diphenylpiperidin-1-yl)-2-buteneHCID 5435232561%

Reaction Steps

A solution of 2,6-diphenylpiperidine [3.0 g, 12.6 mmol; prepared by the method of V. Baliah et al., Indian J. Chem., 16B, 1965 (1978)] and 1,4-but-2-enediol diacetate (1.1 g, 6.3 mmol) in tetrahydrofuran (20 ml, THF) is treated with tetrakis(triphenylphosphine)palladium (0) (0.65 g, 0.6 mmol) and stirred at room temperature overnight. The reaction mixture is concentrated in vacuo to a solid that is redissolved in THF (100 ml) and treated with 20% aqueous sodium hydroxide (25 ml). The mixture is stirred for one hour, concentrated, and extracted with diethyl ether. The ether extracts are dried and concentrated giving an orange solid which is purified by crystallization from methanol to yield 2.02 g (61%) of the title compound as a white solid melting at 197°-200° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05290940
Source datasetuspto-grants-1994_03
ORD IDord-dbc47dccc87e42fe81431cb032d5cf2c
Source noteuspto-grants-1994_03