HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoic Acid → Benzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | HCID 21854354 | HCID 21854354 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | Benzoyl chloride | HCID 7412 | 96% |
Reaction Steps
The procedure described in Example 1 was used and was applied to a solution of 1 mol of benzoic acid in 140 g of xylene. The reaction was carried out in the presence of 10 mmols of N-butyl-4-pyridone. 120 g of phosgene were introduced in the course of 2 hours 40 minutes. The yield obtained after distillation is 98.5%. Infra-red spectrometry did not reveal any trace of benzoic anhydride in the residue. The latter was recycled and a further batch of one mol of benzoic acid was introduced into the reactor. 120 g of phosgene are introduced in the course of 3 hours and the usual cycle is followed. A yield of 96% of benzoyl chloride was obtained after distillation. The residue still showed no traces of anhydride in infra-red spectrometry.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04297301 |
| Source dataset | uspto-grants-1981_10 |
| ORD ID | ord-a73fc58458ef4359b5c314e2ff1fc9f7 |
| Source note | uspto-grants-1981_10 |