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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21908생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/21908

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl cyanoacetateHCID 7764—
반응물TriphenylphosphineHCID 11776—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물Methyl 4-(3-hydroxypropyl)benzoateHCID 14425137—
반응물Methyl-(4-cyano-4-ethoxycarbonylbutyl)benzoateHCID 86748740—
용매TetrahydrofuranHCID 8028—
생성물Methyl 4-(4-cyano-4-ethoxycarbonylbutyl)benzoateHCID 1993089140%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05426110
출처 데이터셋uspto-grants-1995_06
ORD IDord-79485092b152460b8534aa79e42ca71f
출처 메모uspto-grants-1995_06