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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 751552Generated: October 25, 2026

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

https://huagongshe.com/reaction/751552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl diazoacetateHCID 12192—
Reactant1-(5-hydroxy-2H-chromen-6-yl)-propan-1-oneHCID 22482871—
Solvent1,2-DichloroethaneHCID 11—
Product7-Hydroxy-6-propionyl-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-1-carboxylic acid ethyl esterHCID 2130496441.3%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07405310B2
Source datasetuspto-grants-2008_07
ORD IDord-ca988fe12a584240ad4a5af4bdb1dbf3
Source noteuspto-grants-2008_07