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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,6-Diphenylpiperidine | HCID 13010638 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,4-Bis(2,6-diphenylpiperidin-1-yl)-2-butene | HCID 54352325 | 61% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05290940 |
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| Source dataset | uspto-grants-1994_03 |
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| ORD ID | ord-dbc47dccc87e42fe81431cb032d5cf2c |
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| Source note | uspto-grants-1994_03 |
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