HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1,3-Bis(2-ethoxycarbonylethylthio)acetone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Dichloroacetone | HCID 10793 | — |
| Reactant | Ethyl 3-mercaptopropionate | HCID 21625 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1,3-Bis(2-ethoxycarbonylethylthio)acetone | HCID 15885283 | 99.9% |
Reaction Steps
To a stirred solution of 1,3-dichloroacetone (6.85 g, 54 mmol) and ethyl 3-mercaptopropionate (13.9 mL, 108 mmol) in anhydrous tetrahydrofuran (150 mL) was dropwise added triethylamine (15.0 mL, 108 mmol) at 0° C. and stirred at room temperature for 24 h. The solvent was evaporated and the residue was partitioned between water and ethyl acetate. The ethyl acetate phase was washed with 5% hydrochloric acid and then brine, dried over sodium sulfate, and concentrated to dryness, affording 17.4 g of the crude 1,3-bis(2-ethoxycarbonylethylthio)acetone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06030965 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-b18b94d224bd45bdb4587bf9fb75d0ad |
| Source note | uspto-grants-2000_02 |