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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 620236Generated: October 29, 2026

1,4-Dibromobutane → 4-(4-Acetyl-3-hydroxy-2-propylphenoxy)butyl bromide

https://huagongshe.com/reaction/620236

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobutaneHCID 8056—
ReactantPotassium CarbonateHCID 11430—
Reactant2',4'-Dihydroxy-3'-propylacetophenoneHCID 2775198—
CatalystPotassium IodideHCID 4875—
SolventMethyl Ethyl KetoneHCID 6569—
Product4-(4-Acetyl-3-hydroxy-2-propylphenoxy)butyl bromideHCID 1337160234.6%

Reaction Steps

2', 4'-dihydroxy-3'-(n-propyl)acetophenone (19.1 g), 1,4-dibromobutane (48 ml, 0.4 moles), potassium carbonate (13.8 g), and potassium iodide (50 mg) were combined in MEK (300 ml). The reaction mixture was stirred and heated to reflux temperature overnight then cooled to room temperature. The cooled solution was partitioned between ethyl acetate and water. The organic layer was separated, dried over magnesium sulfate, filtered and concentrated in vacuo. The concentrate was chromatographed on a preparatory-scale HPLC (silica column) eluted with a gradient of 1 to 20% ethyl acetate in hexane to yield 11.2 g of the title product: n.m.r. (300 MHz, CDCl3) δ: 12.8 (s, 1H); 7.6 (d, 1H); 6.45 (d, 1H); 4.1 (t, 2H); 3.55 (t, 2H); 2.7 (t, 2H); 2.65 (s, 3H); 2.25 (m, 2H); 2.05 (m, 2H); 1.58 (m, 2H); 0.98 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04820723
Source datasetuspto-grants-1989_04
ORD IDord-71eadbe877d24c7eac95357c874ca528
Source noteuspto-grants-1989_04