HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 4-(Aminosulfonyl)-3-thiophenecarbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 3-Thiophenecarboxylic acid, 4-(aminosulfonyl)- | HCID 3042285 | — |
| Product | 4-(Aminosulfonyl)-3-thiophenecarbonyl chloride | HCID 13732556 | — |
Reaction Steps
A mixture of 1 g. of 4-(aminosulfonyl)-3-thiophenecarboxylic acid in 20 ml of thionyl chloride is heated under reflux for 4 hours. The mixture is cooled to room temperature and is filtered. The filtrate is evaporated in a rotary evaporator and the residue is dissolved in 270 ml. of anhydrous ether. The solution is diluted with 200 ml. of petroleum ether and the precipitate which forms is collected to give 0.4 g. of product, m.p. 140; 262°-265° C.; mass spectrum CI m/e 226 MH+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04621142 |
| Source dataset | uspto-grants-1986_11 |
| ORD ID | ord-940f34b62c524172b0972cfe1d4a3083 |
| Source note | uspto-grants-1986_11 |