HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905301Generated: October 30, 2026
Acetic Anhydride → Ethanone, 1-[4-(acetyloxy)-3-[(acetyloxy)methyl]phenyl]-
https://huagongshe.com/reaction/905301
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 1-[3-(Chloromethyl)-4-hydroxyphenyl]ethan-1-one | HCID 2404811 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Ethanone, 1-[4-(acetyloxy)-3-[(acetyloxy)methyl]phenyl]- | HCID 154871 | — |
Reaction Steps
3'-Chloromethyl-4'-hydroxyacetophenone (108 g.) was added to a mixture of anhydrous sodium acetate (54 g.) glacial acetic acid (500 ml.) and acetic anhydride (250 ml.). The mixture was heated at 95° C. for 4 hours, then concentrated by distilling under reduced pressure. The gummy residue was dissolved in water (500 ml.) and the aqueous solution was extracted with chloroform (3×300 ml.). The combined extracts were dried (MgSO4), filtered and evaporated to give a yellow oil. This was distilled under high vacuum to give 3'-acetoxymethyl-4'-acetoxyacetophenone as a colourless viscous liquid (108 g.), b.p. 143°-147° C. (0.3 mm.), which crystallised on cooling to give solid, m.p. 47°-48° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04423070 |
|---|
| Source dataset | uspto-grants-1983_12 |
|---|
| ORD ID | ord-0312761ab54440afaba556cc06ce23d8 |
|---|
| Source note | uspto-grants-1983_12 |
|---|