HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetone → Ethyl 2-(4-(2-oxopropylthio)phenyl)acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Mercapto-phenyl-acetic acid ethyl ester | HCID 12330043 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 2-(4-(2-oxopropylthio)phenyl)acetate | HCID 66764764 | — |
Reaction Steps
To a solution of (4-mercaptophenyl)-acetic acid ethyl ester (10 g, 0.051 mol) in 150 mL of acetone is added potassium carbonate (anhydrous, 8.51 g, 0.061 mol) at 0° C., followed by dropwise addition of chloroacetone (5 mL, 0.061 mol) in 10 mL of acetone at 0° C. The reaction is then maintained at RT for 2 h. The reaction is filtered and the filtrate is concentrated under vacuum. The residue thus obtained is diluted with 15 mL of water and extracted with ethyl acetate (2×50 mL). The organic layer is then washed with water and brine, dried over sodium sulfate, filtered and evaporated under vacuum to give [4-(2-oxo-propylsulfanyl)-phenyl]-acetic acid ethyl ester as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07781451B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-2a94180bae4f40549d64e03ff205d57c |
| Source note | uspto-grants-2010_08 |