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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 606334Erstellt: 24. Oktober 2026

Ethyl diazoacetate → 7-Hydroxy-6-propionyl-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-1-carboxylic acid ethyl ester

https://huagongshe.com/de/reaction/606334

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl diazoacetateHCID 12192—
Edukt1-(5-hydroxy-2H-chromen-6-yl)-propan-1-oneHCID 22482871—
Lösungsmittel1,2-DichloroethaneHCID 11—
Produkt7-Hydroxy-6-propionyl-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-1-carboxylic acid ethyl esterHCID 2130496441,3%

Reaktionsschritte

To a mixture of 1-(5-hydroxy-2H-chromen-6-yl)-propan-1-one (511 mg, 2.5 mmol) and (Rh(II)Ac2)2 (11 mg, 0.025 mmol) in 1,2-dichloroethane (8 mL) at 20° C., was added dropwise (3 h) a solution of ethyl diazoacetate (571 mg, 5 mmol) in 1,2-dichloroethane (2 mL). After 15 min at 20° C., the reaction mixture was washed with H2O (10 mL). The H2O phase was washed with CH2Cl2 (10 mL) and the solvent of the combined organic phases was removed under reduced pressure. The crude product was purified by column chromatography (silica gel, 1→5% MeOH in CH2Cl2), to give 300 mg (41%) of 7-hydroxy-6-propionyl-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-1-carboxylic acid ethyl ester (a 33/64 mixture of cis and trans isomers).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07915295B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-2f3780e072e9422cbddb27c5267d98c8
Quellennotizuspto-grants-2011_03