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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717801Generated: October 26, 2026

Water → 1-[2-Hydroxy-4-(4-iodo-benzyloxy)-3-propyl-phenyl]-ethanone

https://huagongshe.com/reaction/1717801

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactant4-Iodobenzyl bromideHCID 954258—
Reactant2',4'-Dihydroxy-3'-propylacetophenoneHCID 2775198—
SolventAcetoneHCID 180—
Product1-[2-Hydroxy-4-(4-iodo-benzyloxy)-3-propyl-phenyl]-ethanoneHCID 5743838752.1%

Reaction Steps

Add 1-bromomethyl-4-iodo-benzene (10.00 g, 33.7 mmol) to a solution of 1-(2,4-dihydroxy-3-propyl-phenyl)-ethanone (6.54 g, 33.7 mmol) and cesium carbonate (13.2 g, 40.4 mmol) in acetone (500 mL) and stir. After 48 hours, pour the reaction into water and extract with ethyl acetate. Combine the organic layers, dry with sodium sulfate, filter and concentrate under reduced pressure to give a residue. Purify the residue by flash chromatography eluting with a gradient of ethyl acetate:hexanes to yield the title product as a yellow solid (7.20 g, 52%): 1H NMR (CDCl3) δ 0.95 (t, 3H), 1.56 (sextet, 2H), 2.56 (s, 3H), 2.69 (t, 2H), 5.09 (s, 2H), 6.43 (d, 1H), 7.15 (d, 2H), 7.57 (d, 1H), 7.73 (d, 2H), 12.74 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803938B2
Source datasetuspto-grants-2010_09
ORD IDord-09cfaa4780f2410e86eb6d1b931ffe96
Source noteuspto-grants-2010_09