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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706458Generated: October 30, 2026

4-Benzyloxy-7-hydroxycoumarin → 7-(3-[4-Acetylphenyl]propoxy)-4-benzyloxycoumarin

https://huagongshe.com/reaction/1706458

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Benzyloxy-7-hydroxycoumarinHCID 13408407—
Reactant1-(4-Acetylphenyl)-3-bromopropaneHCID 14817035—
SolventEthanolHCID 702—
Product7-(3-[4-Acetylphenyl]propoxy)-4-benzyloxycoumarinHCID 2033144877%

Reaction Steps

Alkylation of 4-benzyloxy-7-hydroxycoumarin (2.68; 0.01 mole) with 1-(4-acetylphenyl)-3-bromopropane (2.41 g; 0.01 mole) as described in example 45 gave 3.28 g (77%) of title compound of m.p. (EtOH) 117° νmax (mull) 1725, 1682, 1620 cm-1 ; τ(DMSO) 7.92 (2H, m); 7.48(3H, s); 7.18 (2H, m); 5.94(2H, t, J 6.4 Hz); 6.69(2H,s); 6.16 (1H,s); 3.17-2.00(12H,m). (Found; C, 75.14; H, 5.52; C21H24O5 requires; C, 75.68; H, 5.65%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04207335
Source datasetuspto-grants-1980_06
ORD IDord-786bf6c1d13b4a43b240c66f1ce57c6e
Source noteuspto-grants-1980_06