HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478884Generated: October 25, 2026
Triethylamine → 2-((2-Benzoylphenylthio)methyl)butyraldehyde
https://huagongshe.com/reaction/478884
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethylacrolein | HCID 70203 | — |
| Reactant | 2-Mercaptobenzophenone | HCID 3499713 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-((2-Benzoylphenylthio)methyl)butyraldehyde | HCID 22325223 | 64% |
Reaction Steps
To an ice bath cooled solution of 9.76 g (0.116 mole) of 2-ethylacrolein in 40 mL of dry THF was added 24.6 g (0.116 mole) of 2-mercaptobenzophenone in 40 mL of THF followed by 13 g, (0.128 mole) of triethylamine. The reaction mixture was stirred at room temperature for 3 days, diluted with ether, and was washed successively with dilute HCl, brine, and 1 M potassium carbonate. The ether layer was dried over MgSO4 and concentrated in vacuo. The residue was purified by HPLC (10% EtOAc-hexane) to give 22 g (64%) of 11 in the second fraction. An attempt to further purify this material by kugelrohr distillation at 0.5 torr (160-190° C.) gave a fraction (12.2 g) which contained starting material indicating a reversed reaction during distillation. This material was dissolved in ether (100 mL) and was washed with 50mL of 1 M potassium carbonate three times to give 6.0 g of a syrup which was purified by HPLC (10% EtOAc-hexane) to give 5.6 g of pure 11.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06642268B2 |
|---|
| Source dataset | uspto-grants-2003_11 |
|---|
| ORD ID | ord-65e628fab7e4417b981e4e8fa649ae8e |
|---|
| Source note | uspto-grants-2003_11 |
|---|