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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1504385생성일: 2026년 10월 25일

Benzyl mercaptan → 4-(Benzylthio)-2-nitroaniline

https://huagongshe.com/reaction/1504385

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl mercaptanHCID 7509—
반응물1,4-DioxaneHCID 31275—
반응물4-Bromo-2-nitroanilineHCID 70132—
반응물DiisopropylethylamineHCID 81531—
촉매1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매WaterHCID 962—
생성물4-(Benzylthio)-2-nitroanilineHCID 1355099388.2%

반응 조건

온도80 °C

반응 단계

A screw cap vial was charged with 4-bromo-2-nitroaniline (7.00 g, 32.3 mmol), xantphos (0.933 g, 1.613 mmol), tris(dibenzylideneacetone)dipalladium (0) (0.738 g, 0.806 mmol), 1,4-Dioxane (32.3 ml), and DIPEA (11.22 ml, 64.5 mmol). The vial was purged with Argon, sealed and heated to 80° C. for 10 minutes. The reaction was cooled to room temperature and benzyl mercaptan (4.01 ml, 33.9 mmol) was added and the reaction heated at 80° C. for 3 hours. The reaction was cooled to room temperature, diluted with water and extracted with DCM (3×). The combined organics were washed with water and brine, dried over magnesium sulfate, filtered and concentrated. The resulting material was concentrated, dissolved in minimal DCM and purified via column chromatography (silica gel 40 g, gradient elution 0 to 50% EtOAc:Heptane) to afford 4-(benzylthio)-2-nitroaniline (7.43 g, 28.5 mmol, 88% yield). m/z (ESI) 261.2 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09212182B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-1e006f5cddc94ebfac893136c2591d2d
출처 메모uspto-grants-2015_12