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HRID 276128作成日:2026年10月25日

Phenol → Malonate ether

https://huagongshe.com/reaction/276128

反応式

関与物質

役割名称HCID仕込み量
反応物PhenolHCID 996—
反応物1,3-Di-tert-butyl 2-diazopropanedioateHCID 5014600—
触媒Rhodium acetateHCID 168478—
生成物Malonate etherHCID 86757830—

反応手順

Alkylation of phenol E-4 (from Chart E) is accomplished by a carbenoid insertion reaction with di-t-butyl diazomalonate (Synthesis 1974, 347) catalyzed by rhodium acetate (J. Med. Chem. 1995, 38:4270), affording malonate ether I-1. Removal of the t-butyl esters is accomplished with trifluroacetic acid in methylene chloride, and the benzyl ester is removed by hydrogenolysis, affording the desired triacid I-3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06353023B1
出典データセットuspto-grants-2002_03
ORD IDord-9a2c7fa9a7814c1684180d9f7dff7afe
出典メモuspto-grants-2002_03