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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2084323Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/2084323

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
PatentnummerUS06716850B2
Quelldatensatzuspto-grants-2004_04
ORD IDord-17eab2251d8f4d25abf2da1a70de0174
Quellennotizuspto-grants-2004_04