HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-dihydro-7-hydroxy-8-propyl-4H-1-benzopyran-4-one → HCID 19922136, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-dihydro-7-hydroxy-8-propyl-4H-1-benzopyran-4-one | HCID 15318299 | — |
| Reactant | HCID 54182027 | HCID 54182027 | — |
| Product | HCID 19922136 | HCID 19922136 | — |
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-(3-methoxy-3-oxopropyl)-3-[6-[(methylsulfonyl)oxy]hexyl]benzenehexanoic acid methyl ester from the preceding example, followed by saponification, in 16.8% overall yield. The product was a colorless solid, mp 109°-110° C., recrystallized from acetonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05434186 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-2eac43db9cff4893a759138c2dc4faef |
| Source note | uspto-grants-1995_07 |