HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 19037033, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 19037045 | HCID 19037045 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 19037033 | HCID 19037033 | 70.6% |
Reaction Steps
A mixture of 0.9 g of 3,4-dihydro-3-hydroxy-2-methoxymethyl-N,2-dimethyl-6-nitro-2H-1-benzopyran-4-carbothioamide, 0.12 g of p-toluenesulfonic acid monohydrate and 25 ml of toluene was refluxed with heating for 2 hours. Ethyl acetate was added to the mixture. After it was washed with water and dried, the solvent was distilled. The resultant residue was purified according to silica gel column chromatography (developing solution. MeOH:CH2Cl2 =1:99) to obtain 600 mg of 2-methoxymethyl-N,2-dimethyl-6-nitro-2H-1-benzopyran-4-carbothioamide with a melting point of 146°-148° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05646308 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-19ef3bea7c6a42d5aedb68f0c7bbef98 |
| Source note | uspto-grants-1997_07 |