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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 350847Generated: November 1, 2026

Acetic Acid → tert-Butyl 2-[3-[N-(3-hydroxypropyl)aminomethyl]phenoxy]butyrate

https://huagongshe.com/reaction/350847

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-Amino-1-propanolHCID 9086—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantTert-butyl 2-(3-formylphenoxy)butyrateHCID 21090531—
SolventChloroformHCID 6212—
Producttert-Butyl 2-[3-[N-(3-hydroxypropyl)aminomethyl]phenoxy]butyrateHCID 2109053333.3%

Reaction Steps

tert-Butyl 2-(3-formylphenoxy)butyrate (105.1 mg, 0.42 mmol) was dissolved in chloroform (10 ml) at room temperature, and thereto were added 3-amino-1-propanol (0.04 ml, 0.47 mmol), sodium triacetoxyborohydride (134.6 mg, 0.63 mmol) and acetic acid (0.03 ml, 0.51 mmol) in sequential order at the same temperature, and then stirred at room temperature for 24 hours. The reaction mixture was added to a saturated aqueous sodium hydrogencarbonate solution and thereafter extracted by chloroform, to obtain an organic layer. The extracted organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressured. The resultant substance was purified by silica gel column chromatography (chloroform/methanol=10/1), whereby the target compound was obtained as a colorless oil (43.3 mg, 33.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183295B2
Source datasetuspto-grants-2007_02
ORD IDord-04c9ac37f7034908adec7a5aa6165d83
Source noteuspto-grants-2007_02