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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 369364생성일: 2026년 10월 25일

Potassium Phosphate, Tribasic → ethyl (S)-5-[2-(tert-butoxycarbonylamino)-1,2,3,4-tetrahydronaphthalen-7-yl]valerate

https://huagongshe.com/reaction/369364

반응식

참여 물질

역할이름HCID투입량
반응물Potassium Phosphate, TribasicHCID 62657—
반응물Ethyl 4-pentenoateHCID 74786—
반응물9-Borabicyclo(3.3.1)nonaneHCID 78966—
반응물(S)-2-(tert-butoxycarbonylamino)-1,2,3,4-tetrahydronaphthalen-7-yl trifluoromethanesulfonateHCID 18651771—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매1,4-DioxaneHCID 31275—
생성물ethyl (S)-5-[2-(tert-butoxycarbonylamino)-1,2,3,4-tetrahydronaphthalen-7-yl]valerateHCID 8675595545.8%

반응 단계

Ethyl 4-pentenoate (317 mg) was dissolved in tetrahydrofuran (5 ml), and 9-borabicyclo[3.3.1]nonane (302 mg) was added to the solution. After reaction for 15 hours at room temperature with stirring, 1,4-dioxane (9 ml), (S)-2-(tert-butoxycarbonylamino)-1,2,3,4-tetrahydronaphthalen-7-yl trifluoromethanesulfonate (890 mg), tetrakis(triphenylphosphine)palladium (0) (65 mg) and potassium phosphate (716 mg) were added to the reaction mixture, followed by reaction for 15 hours at 85° C. with stirring. Water was added to the reaction mixture, and the resulting mixture was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate, then the solvent was removed in vacuo. Purification by medium pressure liquid column chromatography on silica gel (eluent: dichloromethane) and sequential recrystallization from hexane of the residue gave ethyl (S)-5-[2-(tert-butoxycarbonylamino)-1,2,3,4-tetrahydronaphthalen-7-yl]valerate (387 mg) having a melting point of 65-67° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06136852
출처 데이터셋uspto-grants-2000_10
ORD IDord-ec41396f73a74cf6b46d3bd50a478c3b
출처 메모uspto-grants-2000_10