Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633886Generated: November 1, 2026

Potassium Carbonate → 3-{4-[(1,4-Dioxaspiro[4.5]dec-8-ylamino)methyl]benzoylamino}propionic acid ethyl ester

https://huagongshe.com/reaction/1633886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-Dioxaspiro[4.5]decan-8-oneHCID 567415—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 22502125HCID 22502125—
Solvent1,2-DichloroethaneHCID 11—
Product3-{4-[(1,4-Dioxaspiro[4.5]dec-8-ylamino)methyl]benzoylamino}propionic acid ethyl esterHCID 54005736—

Reaction Conditions

Temperature25 °C

Reaction Steps

1.2 g Ethyl 3-(4-aminomethylbenzoylamino)propanoate hydrochloride (4.18 mmol) was mixed with 20 mL 1,2-dichloroethane and 6 mL saturated K2CO3 by vigorous stirring. The phases were separated and the aqueous phase was extracted with another 20 mL 1,2-dichloroethane. 240 μL HOAc was added to the combined 1,2-dichloroethane phase followed by 0.691 g 1,4-dioxaspiro[4.5]decan-8-one (4.42 mmol). 1.272 g NaBH(OAc)3 (6 mmol) was added and the reaction was stirred for 16 hours at 25° C. The reaction volume was reduced on a rotary evaporator to about 20 mL and then poured into a mixture of 60 mL H2O and 10 mL sat. K2CO3. The phases were separated and the aqueous phase was extracted twice with 40 mL 1,2-dichloroethane. The combined 1,2-dichloroethane fractions were dried over MgSO4 and evaporated to afford the title compound. The crude product was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06503949B1
Source datasetuspto-grants-2003_01
ORD IDord-7f3aafa9800a48a9b5e5a44e6b292c17
Source noteuspto-grants-2003_01