HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210072Generated: October 30, 2026
O-Xylene → 7-(phenylmethoxy)-8-(2-propenyl)-4H-1-benzopyran-4-one
https://huagongshe.com/reaction/2210072
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | 1-[2-Hydroxy-4-(phenylmethoxy)-3-(2-propenyl)phenyl]ethanone | HCID 15048041 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 7-(phenylmethoxy)-8-(2-propenyl)-4H-1-benzopyran-4-one | HCID 19379930 | 67.6% |
Reaction Steps
A mixture of 5.0 g (17.73 mmol) of 1-[2-hydroxy-4-(phenylmethoxy)-3-(2-propenyl)phenyl]ethanone, 2.3 g (19.48 mmol) of dimethylformamide dimethyl acetal, and 5.0 mL of xylene was stirred and heated in a 120°-130° C. oil-bath as methanol was distilled out using a 3 in. Vigreux column, over a 2.5 hr period. The bath temperature was then raised to 150°-160° C. and the reaction mixture was stirred at this temperature for an additional 30 min. The mixture was cooled and concentrated at 60° C./high vacuum. To the viscous, red-brown, oily residue was added 3.7 g (19.48 mmol) of p-toluenesulfonic acid monohydrate and 50 mL of ethanol. The resulting solution was stirred and refluxed for 24 hr, then cooled and diluted with water. Work-up with ether in the usual manner gave a crude product which was recrystallized from hexane-ethyl acetate. There was obtained 3.5 g (67.6%) of 7-(phenylmethoxy)-8-(2-propenyl)-4H-1-benzopyran-4-one as a yellow solid, mp 90°-92° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05457124 |
|---|
| Source dataset | uspto-grants-1995_10 |
|---|
| ORD ID | ord-9b0c91652c9e4e7784496719dd9f3b57 |
|---|
| Source note | uspto-grants-1995_10 |
|---|