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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749922Generated: October 30, 2026

Water → HCID 71278618, compound

https://huagongshe.com/reaction/1749922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-MethylpiperazineHCID 53167—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMethyl 5-chloro-3-formyl-2-(2-methoxy-2-oxoethoxy)benzoateHCID 86682046—
SolventDichloromethaneHCID 6344—
ProductHCID 71278618HCID 7127861892.5%

Reaction Steps

A solution of methyl 5-chloro-3-formyl-2-(2-methoxy-2-oxoethoxy)benzoate (0.99 g, 3.5 mmol) in methylene chloride (30 mL) was added with N-methylpiperazine (0.38 g, 3.8 mmol), and the mixture was stirred at room temperature for 10 minutes. The reaction mixture was cooled to 0° C., and then added portionwise with sodium triacetoxyborohydride (0.12 g, 5.5 mmol). After completion of the addition, the reaction mixture was warmed to room temperature, and stirred for 12 hours. The reaction mixture was added with water, the mixture was extracted with ethyl acetate, and the organic layer was successively washed with saturated aqueous sodium hydrogencarbonate, and saturated brine, and then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was subjected to silica gel column chromatography (eluted with chloroform/methanol (99:1→95:5)) to obtain methyl 5-chloro-2-(2-methoxy-2-oxoethoxy)-3-[(4-methylpiperazin-1-yl)methyl]benzoate (1.2 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-1445c080d298441280c986846686dbaa
Source noteuspto-grants-2015_10