HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → (2-Bromophenyl)(2,2-diethoxyethyl)sulfane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethane, 2-bromo-1,1-diethoxy- | HCID 74852 | — |
| Reactant | 2-Bromobenzenethiol | HCID 80598 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (2-Bromophenyl)(2,2-diethoxyethyl)sulfane | HCID 12045537 | 85.4% |
Reaction Steps
A 500 mL round bottom flask was charged with anhydrous DMF (100 mL), 2-bromothiophenol (10.0 g, 52.88 mmol), potassium carbonate (11.0 g, 79.59 mmol) and bromoacetaldehyde diethyl acetal (8.35 mL, 55.5 mmol). The reaction was stirred at room temperature for 5 hours. Water (50 mL) and ethyl acetate (100 mL) were then added with mixing. The layers were separated and the organic layer was washed with water (5×50 mL), dried over anhydrous sodium sulfate, filtered and concentrated under vacuum to provide 2-(2-bromophenylthio)acetaldehyde diethyl acetal (13.78 g, 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06436964B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-be8e358c75414f23b579d1ecd1111b79 |
| Source note | uspto-grants-2002_08 |