HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → Ethyl 4-(3-bromopropyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-(3-bromopropyl)benzoic acid | HCID 237785 | — |
| Product | Ethyl 4-(3-bromopropyl)benzoate | HCID 12748306 | — |
Reaction Steps
100 g 4-(3-Bromo-propyl)-benzoic acid (JACS 65, 2281 (1943) , 400 ml of toluene and 80 ml of thionyl chloride were refluxed for 4 hours. The solvent and the thionyl chloride in excess were removed under reduced pressure and after addition of 400 ml of absolute ethanol to the residue the mixture was heated for one hour to the boiling point. It was evaporated under reduced pressure, the residue was taken up in benzene and washed neutral with a saturated NaHCO3 -solution. The organic phase was distilled off after drying with MgSO4. Boiling point0.1 : 105° - 107° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04083990 |
| Source dataset | uspto-grants-1978_04 |
| ORD ID | ord-bb5681c071f64926bc95c366d4df30ad |
| Source note | uspto-grants-1978_04 |