Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Benzenesulfenyl chloride | HCID 11008040 | — |
| Reactant | HCID 13363515 | HCID 13363515 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13363535 | HCID 13363535 | 87.6% |
Reaction Steps
Sodium hydride (0.107 g; 60% dispersion in mineral oil) was dispersed in N,N-dimethylformamide (20 ml). To this solution was added isopropyl N-(8-ethoxy-1,3-benzodioxan-6-yl)carbamate (0.75 g) under ice-cooling. After being stirred at room temperature for 1 hour, phenylsulfenyl chloride (0.39 g) was added thereto under ice-cooling, and stirring was continued at room temperature overnight. The resulting mixture was poured into ice-water and extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography using a mixture of toluene and ethyl acetate as the eluent to give isopropyl N-phenylthio-N-(8-ethoxy-1,3-benzodioxan-6-yl)carbamate (Compound 25) (0.91 g) in a yield of 87.5%. M.P., 120°-123° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04686232 |
|---|
| Source dataset | uspto-grants-1987_08 |
|---|
| ORD ID | ord-323422090e9547dfb62757ce11acaab4 |
|---|
| Source note | uspto-grants-1987_08 |
|---|