HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 4-(5-Pentyl-1,3-dioxan-2-YL)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 4-Formylbenzoic acid | HCID 12088 | — |
| Reactant | 2-Pentyl-1,3-propanediol | HCID 117509 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(5-Pentyl-1,3-dioxan-2-YL)benzoic acid | HCID 13561226 | 80.9% |
Reaction Steps
A mixture of 2-n-pentylpropane-1,3diol (8 g, 0.054 m), 4-carboxybenzaldehyde (8 g, 0.053 m), benzene (200 ml) and a catalytic amount of 4-toluenesulfonic acid was azeotropically refluxed until no more water was collected. The cold reaction mixture was washed with saturated NaHCO3 solution and water and then dried over anhydrous sodium sulfate. The solvent was evaporated and the residue was crystallized from ethanol to yield 4-(5-n-pentyl-1,3-dioxan-2-yl) benzoic acid (12 g, 80%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04356104 |
| Source dataset | uspto-grants-1982_10 |
| ORD ID | ord-47393453eab443779abc4ab477b5496d |
| Source note | uspto-grants-1982_10 |