HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-dihydro-7-hydroxy-8-propyl-4H-1-benzopyran-4-one → HCID 19921951, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-dihydro-7-hydroxy-8-propyl-4H-1-benzopyran-4-one | HCID 15318299 | — |
| Reactant | HCID 54121196 | HCID 54121196 | — |
| Product | HCID 19921951 | HCID 19921951 | — |
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 2-[(5-methoxy-4,4-dimethyl-5-oxopentyl)oxy]-6-[6-[(methylsulfonyl)oxy]hexyl]benzenepropanoic acid methyl ester from the preceding example, followed by saponification, in 33.9% overall yield. The product was a colorless solid, mp 85°-87° 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-5d9323a4056e468fbb7c79385c0a63d6 |
| Source note | uspto-grants-1993_12 |