HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 2,4-Dichloro-5-(piperidin-1-ylsulfonyl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,4-Dichloro-5-(chlorosulphonyl)benzoic acid | HCID 77336 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,4-Dichloro-5-(piperidin-1-ylsulfonyl)benzoic acid | HCID 767909 | — |
Reaction Steps
A stirred suspension of 1.7 g. (0.02 mole) of piperidine and 5.8 g. (0.02 mole) of 2,4-dichloro-5-chlorosulfonylbenzoic acid (Sturm, et al., Ber., 99, 328 (1966) in 70 ml. of water and cooled to 15° C. is treated dropwise with 50 ml. of 1N sodium hydroxide. When the addition is complete, the mixture is allowed to warm to room temperature and remain for 1 hr. The hazy suspension is filtered and the clear filtrate acidified with 12N hydrochloric acid. The precipitated solids are filtered and dried, 7.7 g., m.p. 200°-205° C. A sample is recrystallized from acetonitrile, m.p. 205°-206° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04138399 |
| Source dataset | uspto-grants-1979_02 |
| ORD ID | ord-838ac1e4698f46f3a9725ca80e67d461 |
| Source note | uspto-grants-1979_02 |