HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-dihydro-7-hydroxy-8-propyl-4H-1-benzopyran-4-one → HCID 19921934, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-dihydro-7-hydroxy-8-propyl-4H-1-benzopyran-4-one | HCID 15318299 | — |
| Reactant | HCID 54277518 | HCID 54277518 | — |
| Product | HCID 19921934 | HCID 19921934 | — |
Reaction Steps
Using the procedure of example 184, the title compound was prepared in 47% overall yield by alkylation of 2,3-dihydro-7-hydroxy-8-propyl-4H-1-benzopyran-4-one with 2-[(9-methoxy-9-oxononyl)oxy]-6-[6-[(methylsulfonyl)oxy]hexyl]benzenepropanoic acid methyl ester from the preceding example followed by saponification. The diacid product was a colorless solid, mp 63°-65° 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-ce1d88465fde44329180dae15fa6fcfe |
| Source note | uspto-grants-1993_12 |