HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluorobenzoic acid → 2-Fluoro-5-chlorosulfonylbenzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluorobenzoic acid | HCID 9935 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Product | 2-Fluoro-5-chlorosulfonylbenzoic acid | HCID 608984 | — |
Reaction Steps
o-Fluorobenzoic acid is reacted with chlorosulfonic acid by the method of Example 1 to form 2-fluoro-5-chlorosulfonylbenzoic acid. This is reacted with 3,5-dimethylpiperidine by the method of Example 1 to form 2-fluoro-5-(3,5-dimethylpiperidinosulfonyl)benzoic acid. This product (0.0015 mole) is heated to 60° C. with diethylamine (10 ml.) and ethanol (3.0 ml.) to form a clear solution, and the reaction mixture is then heated at reflux temperature for 24 hours. The resulting brown solid is filtered off, dissolved in 1 N NaOH, washed twice with water, and the product precipitated by the addition of concentrated HCl. Recrystallization from diethyl ether replaced by isopropyl ether yields the product, m.p. 139.5°-140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04377521 |
| Source dataset | uspto-grants-1983_03 |
| ORD ID | ord-d99789d8bd1745d0b50601fa6bfd055e |
| Source note | uspto-grants-1983_03 |