HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217789Generated: November 4, 2026
Dichloromethane → 1-Propanone, 2-chloro-1-[4-(phenylmethoxy)phenyl]-
https://huagongshe.com/reaction/2217789
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | p-Benzyloxypropiophenone | HCID 78246 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Propanone, 2-chloro-1-[4-(phenylmethoxy)phenyl]- | HCID 12119195 | 75% |
Reaction Steps
To a methylene chloride solution (20 mL) of 4.80 g (20 mmol) of p-(benzyloxy)propiophenone, 2.97 g (1.1 equivalents) of sulfuryl chloride was added at 15° C., followed by 16 hours of stirring. After 20 mL of water was added, methylene chloride was distilled off under a reduced pressure, and extraction was conducted by adding 40 mL of ethyl acetate. The organic layer was washed with 20 mL of a saturated sodium hydrogen carbonate solution, dried over anhydrous magnesium sulfate, and subjected to distillation under a reduced pressure to remove the solvent. A colorless, oily substance (6.299 g) was thereby obtained. The oily substance was crystallized from 0.5 mL of ethyl acetate and 20 mL of hexane to obtain white crystals of 1-[4-(benzyloxy)phenyl]-2-chloro-1-propanone (4.3787 g, isolation yield: 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07408084B2 |
|---|
| Source dataset | uspto-grants-2008_08 |
|---|
| ORD ID | ord-a417cceb62504998a4845dc7b111d11e |
|---|
| Source note | uspto-grants-2008_08 |
|---|