HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chlorobenzoic Acid → HCID 21393535, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chlorobenzoic Acid | HCID 447 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 4,4,5,5-Tetrachloro-2-methyl-1,2-thiazolidin-3-one | HCID 12324744 | — |
| Solvent | Carbon Dioxide | HCID 280 | — |
| Product | HCID 21393535 | HCID 21393535 | — |
Reaction Steps
To a solution of 2.55g. (0.01 mole) of 2-methyl-4,4,5,5-tetrachloro-3-isothiazolidinone in 10 ml. of chloroform at 0° is added a solution of 2.03g. (0.01 mole) of m-chloroperbenzoic acid (85% Technical) in 60 ml. of chloroform. The mixture is allowed to warm to room temperature and stand over a weekend. The solution is cooled in dry ice. White solid (m-chlorobenzoic acid) separates (0.91g.) and is removed by filtration. The filtrate is washed in a separatory funnel with 50 ml. of water containing 0.4g. of sodium bicarbonate. The chloroform solution is separated and dried over magnesium sulfate. Evaporation gives 2.54g. of crude product as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04062859 |
| Source dataset | uspto-grants-1977_12 |
| ORD ID | ord-009bb48a07424e378f49841748f4b36b |
| Source note | uspto-grants-1977_12 |