HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 2-Phenyl-1,3-dithiane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Boron trifluoride etherate | HCID 8000 | — |
| Reactant | 1,3-Propanedithiol | HCID 8013 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Phenyl-1,3-dithiane | HCID 21547 | — |
Reaction Steps
To a solution of benzaldehyde (15.0 g, 141 mmol) in chloroform (150 mL), propane-1,3-dithiol (16.9 g, 155 mmol) and boron trifluoride etherate (26.1 g, 183 mmol) were added. The reaction mixture was stirred at ambient temperature for 24 h, and was then poured into ice-cold aqueous sodium hydroxide (10%) and extracted with chloroform. The combined chloroform extracts were washed with water, dried over sodium sulfate, concentrated and purified by flash column chromatography using 1% ethyl acetate in hexane as eluent. Yield: 21.2 g, 77%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07910613B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-223d3dfe4de44ec5b90c1d9e81ebb820 |
| Source note | uspto-grants-2011_03 |