HuagongsheHuagongshe Chemistry Print Report · For research reference only
beta-Alanine, ethyl ester, hydrochloride → Ethyl 4-(tert-butyldimethylsilyloxy)-3-(3-ethoxy-3-oxopropylamino)butanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | beta-Alanine, ethyl ester, hydrochloride | HCID 458475 | — |
| Reactant | (E)-4-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-2-butenoic Acid Ethyl Ester | HCID 10490523 | — |
| Reactant | beta-Alanine Hydrochloride | HCID 12201475 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 4-(tert-butyldimethylsilyloxy)-3-(3-ethoxy-3-oxopropylamino)butanoate | HCID 86761499 | 76% |
Reaction Steps
Ethyl 3-aminopropanoate HCl salt (4.6 g, 39.2 mmol, 1.4 eq) was added to a solution of (E)-ethyl 4-(tert-butyldimethylsilyloxy)but-2-enoate in 50 mL of ethanol. The mixture was stirred at RT overnight and then heated to reflux overnight. Another 9.2 g of 3-aminopropanoate HCl salt was added. The reaction was continued to heat at reflux for 2 hr. Solvents were removed; the yellow oily residue was dissolved in DCM, filtered through a pad of SiO2 (˜80 g), and washed with 800 mL EtOAc. The filtrate was concentrated to give the product 7.8 g (76%) as a light yellow liquid. HPLC retention time: T=1.844 min (analytical-3); ESI-MS:m/z 362.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08129538B1 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-3fe8bf8bd6354c8693c5136b349ddfc2 |
| Source note | uspto-grants-2012_03 |