HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dimethoxyethane → 1-(2-Carboxybenzoyl)-2-methyl-4-phenyl-3-thiosemicarbazide, ammonium salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 1-(2-Carboxybenzoyl)-2-methyl-4-phenyl-3-thiosemicarbazide | HCID 12881173 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(2-Carboxybenzoyl)-2-methyl-4-phenyl-3-thiosemicarbazide, ammonium salt | HCID 131712306 | — |
Reaction Steps
The free acid compound of Example 4 was suspended in 100 ml of ethanol and placed in a 300 ml round-bottomed flask equipped with magnetic stirrer and condenser. Twenty ml of dimethoxyethane were added to make the compound go into solution. After most of the solid had gone into solution, NH4OH was added. There was no discernible heat evolution. Solvents were evaporated. The resulting solid (title product) was refluxed in a mixture of hexane and ethanol and was then recovered by filtration. Yield 4.3 g. (m.p. 165°-166°).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04282031 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-45d34ce13f6b44bcb98e13f2464214a4 |
| Source note | uspto-grants-1981_08 |