HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380778Generated: October 31, 2026
HCID 178418361, compound → HCID 178444397, compound
https://huagongshe.com/reaction/1380778
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Reactant | HCID 178444396 | HCID 178444396 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Toluene ethanol | HCID 21863594 | — |
| Product | HCID 178444397 | HCID 178444397 | 70.2% |
Reaction Steps
2.20 g of 4-(trans-4-pentylcyclohexyl)-4'-[2-(trans-4-pentylcyclohexyl)vinyl]biphenyl were suspended in a toluene/ethanol mixture (3:2) in a sulphonation flask, treated with 200 mg of palladium/carbon (10%) and hydrogenated at normal pressure and 50° C. until the hydrogen uptake came to a standstill. Filtration of the mixture and concentration of the filtrate gave a white, semi-crystalline residue which, after recrystallization from 100 ml of hexane, yielded 1.55 g of 4-(trans-4-pentylcyclohexyl)-4'-[2-(trans-4-pentylcyclohexyl)ethyl]biphenyl as colourless needles; transition (presumably S-S) 219.5° C., transition S-N 243.2° C., cl.p. (N-I) 256.1° C. This substance showed itself to be very considerably super-coolable; it did not crystallize upon cooling to room temperature. Rf value (hexane): 0.32.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04583826 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-a1681f30cf124cc7b7465b18fbcc569f |
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| Source note | uspto-grants-1986_04 |
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