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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2040641Erstellt: 24. Oktober 2026

Methanol → Ethyl 3-(3-oxocyclobutyl)propanoate

https://huagongshe.com/de/reaction/2040641

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktAmmonium ChlorideHCID 25517—
EduktEthyl 3-(2,2-dichloro-3-oxocyclobutyl)propanoateHCID 67775324—
KatalysatorZincHCID 23994—
LösungsmittelDiethyl EtherHCID 3283—
ProduktEthyl 3-(3-oxocyclobutyl)propanoateHCID 6777533360,1%

Reaktionsschritte

A solution of ethyl 3-(2,2-dichloro-3-oxocyclobutyl)propanoate (10.49 g, 43.87 mmol) and ammonium chloride (12 g, 220 mmol) in methanol (310 mL, 7600 mmol) was treated in small portions with zinc powder (14 g, 220 mmol). The reaction mixture was heated at reflux for 3 h after which time GC indicated the reaction was complete. The reaction mixture was cooled to room temperature and was filtered through Celite, washing the pad with Et2O. The filtrate was concentrated in vacuo to afford pale yellow solution. The solution was diluted with 200 mL Et2O and washed with 100 mL water. The separated aqueous layer was back extracted with 100 mL Et2O and the combined organic phase was washed with 100 mL 1:1 water/brine, 50 mL water, and 150 mL saturated aqueous NaHCO3. The organic layer was dried over MgSO4, filtered and concentrated in vacuo to afford the title compound (4.49 g, 60%) as a pale yellow oil which was of sufficient purity for use in the next step: GC purity >95% (ret. time, 4.24 min).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08580762B2
Quelldatensatzuspto-grants-2013_11
ORD IDord-489d81febe924e8f8ef77870b12ddc94
Quellennotizuspto-grants-2013_11