HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuryl chloride → 2-Chloro-5-[2-chloro-4-(trifluoromethyl)phenoxy]benzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | 2-Chloro-5-(2-chloro-4-trifluoromethylphenoxy)benzoic acid | HCID 13013682 | — |
| Product | 2-Chloro-5-[2-chloro-4-(trifluoromethyl)phenoxy]benzoyl chloride | HCID 12799632 | 86% |
Reaction Steps
In 100 ml sulfonylchloride was heated 20.0 g (0.057 mol) of 2-chloro-5-(2-chloro-4-trifluoromethylphenoxy)benzoic acid to reflux for 1 hour, and then thionylchloride was removed by distillation. By vacuum distillation of the residue, 18.2 g (0.049 mol) of 2-chloro-5-(2-chloro-4-trifluoromethylphenoxy)benzoyl chloride was obtained; yield 86.0%, b.p. 142°-155° C./0.35 mmHg, nD25 1.5652.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04334914 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-ca3e4616e49141b09e24d94846eca4ad |
| Source note | uspto-grants-1982_06 |