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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221216Generated: October 30, 2026

1,4-Dibromobutane → HCID 57467384, compound

https://huagongshe.com/reaction/221216

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DibromobutaneHCID 8056—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 57467383HCID 57467383—
SolventAcetoneHCID 180—
ProductHCID 57467384HCID 57467384—

Reaction Steps

To a solution of ethyl 2-(4-hydroxy-2-nitrophenoxy)acetate 12 (0.17 g, 0.0007 mol) in 10 mL acetone was added potassium carbonate (0.39 g, 0.0028 mol). The reaction mixture was stirred at room temperature for 10 min. Then 1,4-dibromobutane 13 (0.33 mL, 0.0028 mol) was added. The resulting mixture was heated at reflux for 12 h. The progress of the reaction was monitored by thin layer chromatography (TLC). Acetone was evaporated and the residue was diluted with water, extracted with ethyl acetate and dried over sodium sulfate to give ethyl 2-(4-(4-bromobutoxy)-2-nitrophenoxy)acetate 14 which was purified by silica gel column chromatography using 0-20% gradient of hexane and ethyl acetate. Yellow oil (0.52 g, 92%). 1H NMR (400 MHz, CDCl3): δ 1.26 (t, J=6.8 Hz, 3H); 1.91-1.98 (m, 2H); 2.02-2.09 (m, 2H); 3.48 (t, J=6.8 Hz, 2H); 3.99 (t, J=6.0 Hz, 2H); 4.26 (q, J=6.8 Hz, 2H); 4.70 (s, 2H); 6.99-7.02 (m, 2H); 7.38 (d, J=3.2 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207163B2
Source datasetuspto-grants-2012_06
ORD IDord-93c5126f4e214431a8c07a794aeb6a86
Source noteuspto-grants-2012_06