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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647981Generated: October 27, 2026

2,3-dihydro-7-hydroxy-8-propyl-4H-1-benzopyran-4-one → 5-chloro-2-[5-[(3,4-dihydro-4-oxo-8-propyl-2H-1-benzopyran-7-yl)oxy]pentyloxy]benzenepropanoic acid

https://huagongshe.com/reaction/1647981

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-dihydro-7-hydroxy-8-propyl-4H-1-benzopyran-4-oneHCID 15318299—
Reactant2-[(5-Bromopentyl)oxy]-5-chlorobenzenepropanoic acid methyl esterHCID 54391460—
Product5-chloro-2-[5-[(3,4-dihydro-4-oxo-8-propyl-2H-1-benzopyran-7-yl)oxy]pentyloxy]benzenepropanoic acidHCID 1529500071%

Reaction Steps

Using the procedure of example 4,5-chloro-2-[5-[(3,4-dihydro-4-oxo-8-propyl-2H-1-benzopyran-7-yl)oxy]pentyloxy]benzenepropanoic acid methyl ester, a pale-yellow oil, was prepared in quantitative yield starting from 0.62 g (3 mmol) of 2,3-dihydro-7-hydroxy-8-propyl-4H-1-benzopyran-4-one and 1.21 g (3.33 mmol) of 2-[(5-bromopentyl)oxy]-5-chlorobenzenepropanoic acid methyl ester. Saponification using the procedure of example 4 afforded 1.01 g (71%) of 5-chloro-2-[5-[(3,4-dihydro-4-oxo-8-propyl-2H-1-benzopyran-7-yl)oxy]pentyloxy]benzenepropanoic acid as a colorless solid, mp 101°-103° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05434186
Source datasetuspto-grants-1995_07
ORD IDord-7874f264de3e4694b6d6603af56f1465
Source noteuspto-grants-1995_07