HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Difluorobenzaldehyde → HCID 178445613, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Difluorobenzaldehyde | HCID 588088 | — |
| Reactant | HCID 178445610 | HCID 178445610 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178445613 | HCID 178445613 | 80% |
Reaction Steps
A solution of 2.4 g (0.01 mol) of 2-[2'-(trans-4"-butylcyclohexyl)-ethyl]propane-1,3-diol, 2.8 g (0.01 mol) of 3,4-difluorobenzaldehyde (manufactured by Aldrich) and 0.1 g of TsOH in 50 cm3 of dichloromethane was refluxed for 3 hours over a hot water bath with a Dean-Stark trap. The reaction solution was washed with water and the dichloromethane was distilled off. The residue was recrystallized from a solvent mixture of acetone and methanol to yield 3.0 g (0.008 mol) of trans-2-(3',4'-difluorophenyl)-5-[2'-(trans-4"-butylcyclohexyl)-ethyl]-1,3-dioxane. The phase transition points of this compound, measured by DSC, were: ##STR45## wherein C is the crystal phase, N is the nematic phase, and I is the isotropic liquid phase.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05238599 |
| Source dataset | uspto-grants-1993_08 |
| ORD ID | ord-2175a81275514568906d291049906762 |
| Source note | uspto-grants-1993_08 |