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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1379849생성일: 2026년 10월 25일

Isopropanol → 2'-[(t-Butoxycarbonylamino)methyl]-4-[(t-butyldiphenylsiloxy)methyl]-1,1'-biphenyl

https://huagongshe.com/reaction/1379849

반응식

참여 물질

역할이름HCID투입량
반응물IsopropanolHCID 3776—
반응물Sodium HydroxideHCID 14798—
반응물2-Bromo-N-(tert-butoxycarbonyl)benzylamineHCID 7018300—
반응물(4-(((tert-Butyldiphenylsilyl)oxy)methyl)phenyl)boronic acidHCID 15224568—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매BenzeneHCID 241—
용매WaterHCID 962—
생성물2'-[(t-Butoxycarbonylamino)methyl]-4-[(t-butyldiphenylsiloxy)methyl]-1,1'-biphenylHCID 22008454100%

반응 단계

To a solution of 3.2 g (8.2 mmol) of 4-(t-butyldiphenylsilyoxymethyl)phenylboronic acid (Step C) in 64 mL of benzene was added 2.2 mL of water, 6.4 mL of 5 N aqueous sodium hydroxide, and 8.3 mL of isopropanol. To this mixture was added 180 mg (0.16 mmol) of tetrakis(triphenylphosphine) palladium and 2.20 g (7.81 mmol) of N-(t-butoxycarbonyl)-2-bromobenzylamine (Step D). The resulting mixture was heated under nitrogen at reflux for 2 hours then cooled to room temperature. The reaction mixture was diluted with 100 mL of water, transferred to a separatory funnel and extracted with ether (3×150 mL). The combined ether extracts were washed with saturated aqueous sodium bicarbonate (100 mL) and saturated aqueous sodium chloride (100 mL), dried over magnesium sulfate and filtered. The solvent was removed under vacuum to give a crude product which was purified by column chromatography on silica gel eluting with hexanesthyl acetate (9:1) to afford 4.31 g (100%) of the product as a clear oil. 1H NMR (200 MHz, CDCl3): δ 1.11 (s, 9H), 1.41 (s, 9H), 4.27 (d, 6 Hz, 2H), 4.45 (m, 1H), 4.81 (s, 2H), 7.20-7.49 (m, 14H), 8.72 (m, 4H). FAB-MS: calculated for C35 H41NO3Si 551; found 552 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05672596
출처 데이터셋uspto-grants-1997_09
ORD IDord-a04fa0c255334a9a8bf435bca4ca3519
출처 메모uspto-grants-1997_09