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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64450생성일: 2026년 10월 24일

Ammonium Chloride → methyl 3-[(1S)-1-{[(S)-tert-butylsulfinyl]amino}propyl]benzoate

https://huagongshe.com/ko/reaction/64450

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물methyl 3-[(E)-[(S)-tert-butylsulfinyl]iminomethyl]benzoateHCID 90072367—
반응물HCID 178443585HCID 178443585—
반응물HCID 178467792HCID 178467792—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물methyl 3-[(1S)-1-{[(S)-tert-butylsulfinyl]amino}propyl]benzoateHCID 86713465—

반응 단계

To a solution of 500 mg of methyl 3-[(E)-{[(S)-tert-butylsulfinyl]imino}methyl]benzoate in 12 ml of THF was added 0.50 ml of a 1 M diethylzinc/hexane solution at −78° C., followed by stirring at the same temperature for 5 minutes. 0.80 ml of a 3 M ethylmagnesium bromide/diethyl ether solution was added thereto at −78° C., followed by stirring at the same temperature for 2 hours. To the reaction mixture were added a saturated aqueous ammonium chloride solution and ethyl acetate to carry out a layer separation operation. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 447 mg of methyl 3-[(1S)-1-{[(S)-tert-butylsulfinyl]amino}propyl]benzoate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447090B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-bfc183d973b3464fa90f16ef138d3c7f
출처 메모uspto-grants-2016_09