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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1,4-Dioxaspiro[4.5]decan-8-one | HCID 567415 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 22502125 | HCID 22502125 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 3-{4-[(1,4-Dioxaspiro[4.5]dec-8-ylamino)methyl]benzoylamino}propionic acid ethyl ester | HCID 54005736 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06503949B1 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-7f3aafa9800a48a9b5e5a44e6b292c17 |
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| Source note | uspto-grants-2003_01 |
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