HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173779Generated: October 26, 2026
Sulfuryl chloride → Ethyl 2-chloro-3-oxo-4-phenylbutyrate
https://huagongshe.com/reaction/1173779
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Ethyl 3-oxo-4-phenylbutanoate | HCID 225855 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-chloro-3-oxo-4-phenylbutyrate | HCID 11601176 | 86.8% |
Reaction Steps
Ethyl 3-oxo-4-phenylbutyrate (4.8 g, 23 mmol) and methylene chloride (48 ml) were mixed, and sulfuryl chloride (3.1 g, 1 equivalent) was gradually added thereto dropwise. After the addition, the mixture was stirred at 20° C. for 1 hour. The reaction mixture was concentrated under reduced pressure, and saturated aqueous solution of sodium hydrogencarbonate (10 ml) was added, and extraction was carried out with ethyl acetate (20 ml). The solvent was evaporated away under reduced pressure and drying was carried out in vacuum to obtain the title compound as a yellow oil (4.8 g, yield: 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07834190B2 |
|---|
| Source dataset | uspto-grants-2010_11 |
|---|
| ORD ID | ord-e6baa6b5b8594ff7abbfbb4adeb29779 |
|---|
| Source note | uspto-grants-2010_11 |
|---|