HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → 1-Benzyl-3-phenylsulfinylindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(Benzenesulfinyl)-1H-indole | HCID 13442934 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Benzyl-3-phenylsulfinylindole | HCID 13442935 | — |
Reaction Steps
This compound was prepared in the same manner as described in Example 7 using sodium hydride (0.036 g, 50% in mineral oil; 0.90 mmol), dimethylformamide (5 ml), 3-phenylsulfinylindole (0.200 g, 0.82 mmol) and benzyl bromide (0.11 ml, 0.154 g, 0.90 mmol). Crystallization of the crude product from dichloromethane-hexane gave the title compound. M.P.-148°-149° (dichloromethane-hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04654360 |
| Source dataset | uspto-grants-1987_03 |
| ORD ID | ord-676c586b4a3449599bff0718ba0bf9ff |
| Source note | uspto-grants-1987_03 |