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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1590798Generated: October 30, 2026

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

https://huagongshe.com/reaction/1590798

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 numberUS05204474
Source datasetuspto-grants-1993_04
ORD IDord-57f9b17eac8e4ab8b6b9ee4b6028c6c3
Source noteuspto-grants-1993_04