HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292214Generated: November 1, 2026
Diethyl Ether → [4-(Acetyloxy)-2-hydroxy-3-propylphenyl][2(acetyloxy)phenyl]methanone
https://huagongshe.com/reaction/2292214
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Dimethylaminopyridine | HCID 21885 | — |
| Reactant | HCID 14421654 | HCID 14421654 | — |
| Product | [4-(Acetyloxy)-2-hydroxy-3-propylphenyl][2(acetyloxy)phenyl]methanone | HCID 21277006 | — |
Reaction Steps
Five grams of (2,4-dihydroxy-3-propylphenyl)- (2-hydroxyphenyl)methanone, 5.63 ml of triethylamine, and approximately 50 mg of dimethylaminopyridine were dissolved in 50 ml of diethyl ether at 0° C. Acetic anhydride (3.8 ml) was added dropwise. After stirring for 1 hour, the reaction mixture was partitioned between diethyl ether and water. The organic layer was separated, washed with 1N hydrochloric acid, a saturated solution of sodium bicarbonate, and a saturated solution of sodium chloride, dried over magnesium sulfate, and concentrated in vacuo. Purification by high pressure liquid chromatography over silica gel eluting with a 10-25% ethyl acetate in hexane gradient and concentration of the appropriate fractions provided 2.6 g of the desired title product as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04801616 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-b506f0a93f454478842c6ee5fb111de7 |
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| Source note | uspto-grants-1989_01 |
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