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 | Dichloromethane | HCID 6344 | — |
| Product | 2-Phenyl-1,3-dithiane | HCID 21547 | 87% |
Reaction Steps
To a solution of benzaldehyde (10.6 g, 100 mmol) and 1,3-propane dithiol in CH2Cl2 (150 mL) at room temperature was dropwise added BF3.Et2O (6.3 mL, 50 mmol) and the resulting mixture was stirred at room temperature for 2 hours. The reaction mixture was then diluted with CH2Cl2, filtered and the filtrate washed with brine, saturated NaHCO3, brine and dried over Na2SO4. The solvent was removed under reduced pressure to afford a white solid, which was recrystallized from a 1:1 mixture of ether and hexane to afford 17.0 g (87%) of the title compound (65) as white crystalline needles. 1H NMR (CDCl3, 400 MHz): δ 1.91 (m, 1H), 2.14 (m, 1H), 2.89 (m, 2H), 3.04 (m, 2H), 5.16 (s, 1H), 7.35-7.28 (m, 3H), 7.46 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08367722B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-f472770636b44d42a59342f290c22ba6 |
| Source note | uspto-grants-2013_02 |