HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648606Generated: November 1, 2026
(1,1'-Biphenyl)-4-carboxaldehyde → 4-Methylbiphenyl
https://huagongshe.com/reaction/1648606
Participants
| Role | Name | HCID | Charge |
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| Reactant | (1,1'-Biphenyl)-4-carboxaldehyde | HCID 76689 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 4-Methylbiphenyl | HCID 12566 | — |
Reaction Steps
5 g/hr of the solution dissolved 10% by weight of 4-formylbiphenyl in a benzene was continuously fed in the hydrogenation reactor, while keep the hydrogen pressure under 10 atm and the reaction temperature at 130° C. Product water was removed from the reaction product solution by phase separation and then benzene was distilled off to obtain 4-methylbiphenyl. The conversion of 4-formylbiphenyl was 99.3% and the selectivity to 4-methylbiphenyl was 99.0% by mole. A small amount of 4-biphenylmethanol and high boiling point products was further contained in 4-methylbiphenyl. Product water was separated from the reaction product solution and then the 4-biphenylmethanol and high boiling point by-products were removed by distillation, whereby 4-methylbiphenyl with a purity of 98% by weight or above was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05436374 |
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| Source dataset | uspto-grants-1995_07 |
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| ORD ID | ord-7e99f2d201db49819349217cf2ec9d3a |
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| Source note | uspto-grants-1995_07 |
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