HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → p-(5-n-Octyl-1,3-dioxan-2-yl)phenyl p-n-butylbenzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 4-Butylbenzoyl chloride | HCID 120049 | — |
| Reactant | p-(5-n-Octyl-1,3-dioxan-2-yl)phenol | HCID 20342141 | — |
| Solvent | Water | HCID 962 | — |
| Product | p-(5-n-Octyl-1,3-dioxan-2-yl)phenyl p-n-butylbenzoate | HCID 20342143 | 51.9% |
Reaction Steps
A mixture of 4-n-butylbenzoyl chloride (0.98 g. 0.005 m), p-(5-n-octyl-1,3-dioxan-2-yl)phenol (1.37 g, 0.005 m), benzene (40 ml) and pyridine (2 ml) was stirred at room temperature for six hours. The resulting reaction mixture was poured into cold water. The organic layer was separated and washed with diluted hydrochloric acid solution, diluted potassium hydroxide solution and water, then dried over anhydrous sodium sulfate. The solvent was evaporated and the residue was crystallized from ethanol to yield p-(5-n-octyl-1,3-dioxan-2-yl)phenyl p-n-butylbenzoate (1.1 g. 51%) CN 65.5°-66.5° C., NL 141°-142° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04200580 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-e77cc3d4c33946898159d67c923c5c54 |
| Source note | uspto-grants-1980_04 |