HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid monohydrate → N-methyl-6-cyano-2,2-dimethyl-2H-1-benzopyran-4-carbothioamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 15054561 | HCID 15054561 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-methyl-6-cyano-2,2-dimethyl-2H-1-benzopyran-4-carbothioamide | HCID 15054568 | — |
Reaction Steps
A mixture of 0.44 g of N-methyl-6-cyano-3,4-dihydro-3-hydroxy-2,2-dimethyl-2H-1-benzopyran-4-carbothioamide, 0.07 g of p-toluenesulfonic acid monohydrate, and 30 ml of toluene was heated at reflux for 10 hours. The solvent was removed by distillation, and the residue was purified by silica gel column chromatography (developing solution: CH2Cl2) to obtain 0.18 g of-N-methyl-6-cyano-2,2-dimethyl-2H-1-benzopyran-4-carbothioamide represented by formula shown below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05412117 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-5032214252f7423c99baac7bb571e4d2 |
| Source note | uspto-grants-1995_05 |