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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 230585생성일: 2026년 10월 26일

Sodium borohydride → N-[4-((1R)-1-{[(R)-tert-butylsulfinyl]amino}ethyl)-2-methylphenyl]methanesulfonamide

https://huagongshe.com/reaction/230585

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참여 물질

역할이름HCID투입량
반응물Sodium borohydrideHCID 4311764—
반응물tert-Butylsulfinamide, (R)-(+)-HCID 10964479—
반응물N-(4-Acetyl-2-methylphenyl)methanesulfonamideHCID 19873430—
촉매Titanium tetraethoxideHCID 76524—
용매TetrahydrofuranHCID 8028—
생성물N-[4-((1R)-1-{[(R)-tert-butylsulfinyl]amino}ethyl)-2-methylphenyl]methanesulfonamideHCID 5864040445.5%

반응 조건

온도70 °C

반응 단계

To a solution of titanium(IV) ethoxide (1.32 g, 5.8 mol) and N-(4-acetyl-2-methylphenyl) methanesulfonamide (800 mg, 3.5 mmol) in tetrahydrofuran (20 mL) was added (R)-(+)-2-methyl-2-propanesulfinamide (423 mg, 350 mmol) under a nitrogen atmosphere and the mixture was heated at 70° C. for 16 hours. It was quenched with water and the resulting white precipitate was filtered off. The filtrate was partitioned between ethyl acetate and water. The organic layer was dried over sodium sulfate and concentrated in vacuo. The crude material was purified by silica gel column chromatography, eluting with hexane/ethyl acetate (4:1). The yellow oil obtained was dissolved in tetrahydrofuran (10 mL) and the solution was added to sodium borohydride (242 mg, 6.4 mmol) in tetrahydrofuran (10 mL) at −70° C. The mixture was stirred at −70° C. for 5 hours and then quenched with methanol. It was stirred at room temperature for 1 hour and concentrated in vacuo to furnish 530 mg (45%) of the title compound. MS (ESI) m/z 333 (M+H)+, 331 (M−H)−.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07566739B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-7919c91fd68a426cb45669c1a7f2747c
출처 메모uspto-grants-2009_07