HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → HCID 12787791, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | p-Bromobenzhydryl alcohol | HCID 98221 | — |
| Reactant | 1-Benzyl-4-bromobenzene | HCID 236000 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 12787791 | HCID 12787791 | 86% |
Reaction Steps
α,α′-Diphenyl-α-hydroxyl-p-xylene was prepared as shown in Scheme 4 by using 29.0 g (117 mmol) of 4-bromo diphenylmethane and 11.2 g (106 mmol) of benzaldehyde/19.7 g (106 mmol) by the similar procedure to the method for preparing 4-bromobenzhydrol. The crude product was dissolved in chloroform and filtered through G60 column filled with silica gel. After evaporating the solvent, the result product was recrystallized with hexane/chloroform (9:1 v/v) to provide a yield of 86%. MP: 64° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829155B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-7766ab21459b46588f604b233799d610 |
| Source note | uspto-grants-2014_09 |