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HRID 21908作成日:2026年10月26日

Ethyl cyanoacetate → Methyl 4-(4-cyano-4-ethoxycarbonylbutyl)benzoate

https://huagongshe.com/reaction/21908

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl cyanoacetateHCID 7764—
反応物TriphenylphosphineHCID 11776—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物Methyl 4-(3-hydroxypropyl)benzoateHCID 14425137—
反応物Methyl-(4-cyano-4-ethoxycarbonylbutyl)benzoateHCID 86748740—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 4-(4-cyano-4-ethoxycarbonylbutyl)benzoateHCID 1993089140%

反応手順

Preparation of methyl-(4-cyano-4-ethoxycarbonylbutyl)benzoate ##STR21## To a 250 mL flame dried round bottom flask were charged 10.0 g (51.5 mmol) of methyl 4-(-hydroxypropyl)benzoate and 5.48 mL (51.5 mmol) of ethyl cyanoacetate dissolved in 40 mL of anhydrous tetrahydrofuran (THF). To this solution was then added dropwise to a solution of 20.2 g (77 mmol) of triphenylphosphine and 12.1 mL (77 mmol) of diethyl azodicarboxylate dissolved in 60 mL of anhydrous THF. After the addition, the reaction was stirred at ambient temperature for 1.5 hours. The volatiles were removed in vacuo and the crude oil was dissolved in 300 mL of EtOAc, washed with brine, dried over Na2SO4, and removed in vacuo. This crude oil was then purified on silica gel using a Waters Prep LC 2000 eluting with a gradient of 1:1 MeCl2 /Hex to 100% MeCl2 to give 6.0 g (40%) of methyl 4-(4-cyano-4-ethoxycarbonylbutyl)benzoate as a pale yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05426110
出典データセットuspto-grants-1995_06
ORD IDord-79485092b152460b8534aa79e42ca71f
出典メモuspto-grants-1995_06