HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Propanedithiol → HCID 10104703, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Propanedithiol | HCID 8013 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | o-Fluorobenzaldehyde | HCID 67970 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10104703 | HCID 10104703 | 78.2% |
Reaction Steps
To a solution of 2-fluorobenzaldehyde (10.03 g, 80.8 mmol, 1.0 eq.) and NBS (2.16 g, 12.1 mmol, 0.2 eq.) in CH2Cl2 (400 mL) was added 1,3-propanedithiol (9.8 mL, 97.6 mmol, 1.2 eq.). After 0.75 h, the reaction mixture was concentrated in vacuo. The residue was diluted with CH2Cl2 and water, and the layers were separated. The organic layer was dried over Na2SO4, filtered, concentrated in vacuo, and triturated with hexanes to give 2-(2-fluorophenyl)-1,3-dithiane as a white solid (13.55 g, 78% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07994337B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-35dfa3b325754d518589164e578e43c9 |
| Source note | uspto-grants-2011_08 |