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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1167146Erstellt: 27. Oktober 2026

Methanol → Methyl 3-amino-3-(3-nitrophenyl)propanoate

https://huagongshe.com/reaction/1167146

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktSulfuric AcidHCID 1118—
Edukt3-Amino-3-(3-nitrophenyl)propanoic acidHCID 237320—
ProduktMethyl 3-amino-3-(3-nitrophenyl)propanoateHCID 276947262%

Reaktionsschritte

A solution of 79.5 g (0.378 mol) D, 3-amino-3-(3-nitrophenyl)propionic acid, in 21 of methanol is admixed with 200 ml of sulphuric acid (conc.). The solution is heated at boiling point for 1 h. Most of the methanol is removed under reduced pressure and the residue is poured into ice-water. Using sodium carbonate, the pH is adjusted to 8. The aqueous phase is extracted with dichloromethane. Drying of the organic phase and removal of the solvent under reduced pressure gives the ester E, methyl 3-amino-3-(3-nitrophenyl)propionate, (52.8 g, 62%) as a white solid. 10 g (44.6 mmol) of E are dissolved in 20 ml of DMF. The solution is admixed with 12.3 g (88.2 mmol) of potassium carbonate, and 15.2 g (88.2 mmol) of benzyl chloroformate are added dropwise. The mixture is stirred at 23° C. for 2 h. The mixture is diluted with 200 ml of toluene and washed three times with water, and the organic phase is dried using sodium sulphate and concentrated under reduced pressure to give the colourless oil of methyl 3-benzyloxycarbonylamino-3-(3-nitrophenyl)propionate (12.6 g, 79%). MS (DCI/NH3): 376 (M+NH4)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06617332B1
Quelldatensatzuspto-grants-2003_09
ORD IDord-275285f946ec44819926e15d1756e3b1
Quellennotizuspto-grants-2003_09