HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanethiol → 4-Chloro-3-(methylsulphenyl)-2-(methylsulphonyl)benzoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanethiol | HCID 878 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | 4-Chloro-3-fluoro-2-methylsulphonylbenzoic acid | HCID 54442430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Chloro-3-(methylsulphenyl)-2-(methylsulphonyl)benzoic acid | HCID 53633451 | 55% |
Reaction Steps
Lithium hydroxide monohydrate (1.26 g) was added to a solution of methyl mercaptan (0.72 g) in dimethyl formamide. To this mixture was added 4-chloro-3-fluoro-2-(methylsulphonyl)benzoic acid (3.7 g). The mixture was stirred for 2 hours then poured into water and acidified to pH1. It was extracted with ether, washed with water, dried (Na2SO4) and filtered. The filtrate was evaporated to dryness and the residue was triturated with n-hexane and filtered to give 4-chloro-3-(methylsulphenyl)-2-(methylsulphonyl)benzoic acid (2.26 g) as a white solid, NMR (CDCl3) 2.5(s,3H), 3.45(s,3H), 7.5(d,1H), 7.7(d,1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05856274 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-4eb30192f8e248068641c6975323a920 |
| Source note | uspto-grants-1999_01 |