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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 486487생성일: 2026년 10월 24일

Acetonitrile → Methyl (RS)-4-cyano-2-phenylbutanoate

https://huagongshe.com/ko/reaction/486487

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Ammonium ChlorideHCID 25517—
반응물Methyl atropateHCID 193334—
반응물Lithium diisopropylamideHCID 2724682—
용매TetrahydrofuranHCID 8028—
용매CyclohexaneHCID 8078—
생성물Methyl (RS)-4-cyano-2-phenylbutanoateHCID 5364509475%

반응 단계

Lithium diisopropylamide (3.67 ml of a 1.5 molar solution in cyclohexane) was added to acetonitrile (0.26 ml) in tetrahydrofuran (10 ml) at -78° C. After 1 hour, methyl 2-phenyl-acrylate (see Preparation 22) (0.81 g) in tetrahydrofurn (10 ml) was added and the mixture was stirred for 1 hour, allowed to warm to room temperature then treated with saturated ammonium chloride solution. The resulting mixture was partitioned between ethyl acetate and water, the organic phase dried over magnesium sulphate and evaporated to give a residue which was partitioned between ether and 10% aqueous sodium carbonate. The organic layer was dried over magnesium sulphate and evaporated to leave the title compound (0.5 g, 75%) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05292749
출처 데이터셋uspto-grants-1994_03
ORD IDord-80af75f55504407f8422051aeb00f6fc
출처 메모uspto-grants-1994_03