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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220844Generated: October 30, 2026

3,3-Dimethylbutanal → 4-{2-[4-(3,3-Dimethyl-butyl)-piperazin-1-yl]-ethoxy}-3-methyl-benzoic Acid Methyl Ester

https://huagongshe.com/reaction/220844

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,3-DimethylbutanalHCID 76335—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant3-Methyl-4-(2-piperazin-1-yl-ethoxy)-benzoic Acid Methyl Ester DihydrochlorideHCID 67053806—
SolventAcetic acid methanolHCID 10129899—
Product4-{2-[4-(3,3-Dimethyl-butyl)-piperazin-1-yl]-ethoxy}-3-methyl-benzoic Acid Methyl EsterHCID 5755521134%

Reaction Steps

3,3-Dimethylbutyraldehyde (54 mg, 0.53 mmol) was added to a solution of 3-methyl-4-(2-piperazin-1-yl-ethoxy)-benzoic acid methyl ester dihydrochloride from Example E40.2 (146 mg, 0.42 mmol) in methanol/acetic acid (99:1, v/v, 10 ml) and the mixture was stirred at room temperature for 1 h. Sodium cyanoborohydride (42 mg, 0.69 mmol) was added, and the mixture was stirred at room temperature for 18 h then concentrated in vacuo. The residue was dissolved in EtOAc, washed with saturated NaHCO3, water then brine, dried and concentrated in vacuo. The residue was purified by flash chromatography on silica gel through an isolute (eluant; EtOAc) to yield the title compound (64 mg, 34%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202858B2
Source datasetuspto-grants-2012_06
ORD IDord-ec7264c6e02a429682a23e3cc7306a2b
Source noteuspto-grants-2012_06