HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → p-(5-n-Butyl-1,3-dioxan-2-yl)phenyl p-n-butylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2-n-Butylpropane-1,3-diol | HCID 2795259 | — |
| Reactant | p-(4'-n-Butylbenzoyloxy)benzaldehyde | HCID 5231030 | — |
| Solvent | Water | HCID 962 | — |
| Product | p-(5-n-Butyl-1,3-dioxan-2-yl)phenyl p-n-butylbenzoate | HCID 15681131 | 67.7% |
Reaction Steps
A mixture of 2-n-butylpropane-1,3-diol (6.6 g, 0.05 m) and p-(4'-n-butylbenzoyloxy)benzaldehyde (14.2 g, 0.05 m), benzene (100 ml) and a catalytic amount of 4-toluenesulfonic acid was azeotropically refluxed until no more water was collected. The solvent was evaporated and the residue was crystallized from ethanol to yield p-(5-n-butyl-1,3-dioxan-2-yl)phenyl p-n-butylbenzoate (13.4 g 67%) CN 79.2°-80.2° C., NL 160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04200580 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-a40763117d874804ba6751f7b4ae4843 |
| Source note | uspto-grants-1980_04 |