HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1-Dibromoethane → 8-(2-Bromoethoxy)-3,4-dihydro-2H-1-benzothiopyran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1-Dibromoethane | HCID 11201 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3,4-dihydro-2H-1-benzothiopyran-8-ol | HCID 121617 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 8-(2-Bromoethoxy)-3,4-dihydro-2H-1-benzothiopyran | HCID 15295832 | — |
Reaction Steps
Tetrabutylammonium bromide (1.94 g 6 mmol; 0.2 eq.), phase-transfer agent, is added to a heterogeneous mixture composed of 8-hydroxy-3,4-dihydro-2H-1-benzothiopyran (5 g; 30 mmol), acetonitrile (30 ml) and a 1.6N sodium hydroxide solution (28.3 ml; 45 mmol; 1.5 eq.). Dibromoethane (10 ml; 60 mmol; 1.5 eq.) is added after 30 minutes' stirring, the stirring being continued for 24 hours at 30° C. Concentration of the various phases under reduced pressure at 25° C. is followed by extraction of the products with dichloromethane. Washing with a 5% sodium hydroxide solution allows a first purification, which is followed by purification over a silica column eluted with a 3:7 AcOEt/PE mixture, yielding the brominated title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05919814 |
| Source dataset | uspto-grants-1999_07 |
| ORD ID | ord-a78f46b20ff94f0681878b90bac417de |
| Source note | uspto-grants-1999_07 |