HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1,1-Trimethoxy-2-methylpropane → N-(1-Methoxy-2-methylpropylidene)-3-phenyl-1,2,4-thiadiazole-5-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1,1-Trimethoxy-2-methylpropane | HCID 40495 | — |
| Reactant | 3-Phenyl-1,2,4-thiadiazole-5-sulfonamide | HCID 14183132 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | N-(1-Methoxy-2-methylpropylidene)-3-phenyl-1,2,4-thiadiazole-5-sulfonamide | HCID 53780129 | — |
Reaction Steps
A mixture of 3 g of 3-phenyl-1,2,4-thiadiazole-5-sulfonamide and and 11 ml of trimethyl orthoisobutyrate was warmed to about 90° using an oil bath. After 2.5 hours, the solution was allowed to cool to room temperature, whereupon a precipitate formed. Hexane (25 ml) was added to complete the precipitation. The solid was collected, washed with hexane and vacuum dried (P2O5) to give 3.34 g of solid, m.p. 123°-124°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04873239 |
| Source dataset | uspto-grants-1989_10 |
| ORD ID | ord-15425112a26b407ebfdbc81d724cd90f |
| Source note | uspto-grants-1989_10 |