HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → HCID 13340179, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 6-Chlorohexanoic acid | HCID 20209 | — |
| Catalyst | p-Toluenesulfonic acid | HCID 6101 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 13340179 | HCID 13340179 | 85.2% |
Reaction Steps
46.5 g (0.3 mole) of 6-chlorohexanoic acid and 35.6 g of benzyl alcohol in 500 ml of toluene are heated in the presence of 1 g of p-toluenesulphonic acid, using a water separator. When the reaction has ended, the mixture is washed with 5% strength sodium bicarbonate solution and water, dried with sodium sulphate and concentrated and the residue is distilled, 61.5 g (85% of theory) of benzyl 6-chlorohexanoate of boiling point 163° to 165°/4 mm being obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04563448 |
| Source dataset | uspto-grants-1986_01 |
| ORD ID | ord-d8975fe5f31e40dc90c467433ad4ab0e |
| Source note | uspto-grants-1986_01 |