HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-dihydro-7-hydroxy-8-propyl-4H-1-benzopyran-4-one → 3-(2-Carboxyethyl)-4-[5-[(3,4-dihydro-4-oxo-8-propyl-2H-1-benzopyran-7-yl)oxy]pentyloxy]-gamma-oxobenzenebutanoic Acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-dihydro-7-hydroxy-8-propyl-4H-1-benzopyran-4-one | HCID 15318299 | — |
| Reactant | 4-[(5-Bromopentyl)oxy]-3-(3-ethoxy-3-oxopropyl)-gamma-oxobenzenebutanoic Acid Ethyl Ester | HCID 54067431 | — |
| Solvent | Ethanol ethylacetate | HCID 21584252 | — |
| Product | 3-(2-Carboxyethyl)-4-[5-[(3,4-dihydro-4-oxo-8-propyl-2H-1-benzopyran-7-yl)oxy]pentyloxy]-gamma-oxobenzenebutanoic Acid | HCID 19921965 | 63.8% |
Reaction Steps
Starting with 0.156 g (0.76 mmol) of 2,3-dihydro-7-hydroxy-8-propyl-4H-1-benzopyran-4-one, and 0.357 g (0.76 mmol) of 4-[(5-bromopentyl)oxy]-3-(3-ethoxy-3-oxopropyl)-γ-oxobenzenebutanoic acid ethyl ester, the title compound (0.237 g; 63.8% overall yield) was obtained as a white solid, mp 181.5°-184° C. (recrystallized from ethanol-ethyl acetate), using the procedure of example 22.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05434186 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-db214d03b0ca4291822bb5967590c65f |
| Source note | uspto-grants-1995_07 |