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HRID 751552作成日:2026年10月26日

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

https://huagongshe.com/reaction/751552

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl diazoacetateHCID 12192—
反応物1-(5-hydroxy-2H-chromen-6-yl)-propan-1-oneHCID 22482871—
溶媒1,2-DichloroethaneHCID 11—
生成物7-Hydroxy-6-propionyl-1,1a,2,7b-tetrahydro-cyclopropa[c]chromene-1-carboxylic acid ethyl esterHCID 2130496441.3%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07405310B2
出典データセットuspto-grants-2008_07
ORD IDord-ca988fe12a584240ad4a5af4bdb1dbf3
出典メモuspto-grants-2008_07