HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-dihydro-7-hydroxy-8-propyl-4H-1-benzopyran-4-one → HCID 19922135, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-dihydro-7-hydroxy-8-propyl-4H-1-benzopyran-4-one | HCID 15318299 | — |
| Reactant | HCID 54096842 | HCID 54096842 | — |
| Product | HCID 19922135 | HCID 19922135 | — |
Reaction Steps
Using the procedure of example 126, 2,3-dihydro-7-hydroxy-8-propyl-4H-1-benzopyran-4-one was converted into the title compound by alkylation with 4-[5-(methylsulfonyl)oxypentyloxy]-1,3-benzenedipropanoic acid methyl ester from the preceding exapmle, followed by saponification, in 8% overall yield. The product was a colorless solid, mp 108°-109° C., recrystallized from hexane-ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05273999 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-ee17ffed7da247d48cb5a03c5fcb28cb |
| Source note | uspto-grants-1993_12 |