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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648063Generated: October 26, 2026

2,3-dihydro-7-hydroxy-8-propyl-4H-1-benzopyran-4-one → 6-{2-(2-Carboxy-ethyl)-3-[6-(4-oxo-8-propyl-chroman-7-yloxy)-hexyl]-phenoxy}-hexanoic acid

https://huagongshe.com/reaction/1648063

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-dihydro-7-hydroxy-8-propyl-4H-1-benzopyran-4-oneHCID 15318299—
Reactant2-[(6-Methoxy-6-oxohexyl)oxy]-6-[6-(methylsulfonyl)oxyhexyl]benzenepropanoic acid methyl esterHCID 54280331—
Product6-{2-(2-Carboxy-ethyl)-3-[6-(4-oxo-8-propyl-chroman-7-yloxy)-hexyl]-phenoxy}-hexanoic acidHCID 9850974—

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-[(6-methoxy-6-oxohexyl)oxy]-6-[6-(methylsulfonyl)oxyhexyl]benzenepropanoic acid methyl ester from the preceding example, followed by saponification, in 79% overall yield. The product was a colorless solid, mp 86°-88° C., recrystallized from hexane-ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05434186
Source datasetuspto-grants-1995_07
ORD IDord-e03d2897a8a64d9783ce2a26cc04cf8f
Source noteuspto-grants-1995_07