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HRID 1080744생성일: 2026년 10월 27일

Tetrabutylammonium Fluoride → 2'-[(t-Butoxycarbonylamino)methyl]-1,1-biphenyl-4-methanol

https://huagongshe.com/reaction/1080744

반응식

참여 물질

역할이름HCID투입량
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물2'-[(t-Butoxycarbonylamino)methyl]-4-[(t-butyldimethylsiloxy)-methyl]-1,1'-biphenylHCID 23365448—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물2'-[(t-Butoxycarbonylamino)methyl]-1,1-biphenyl-4-methanolHCID 2200847293%

반응 단계

To a solution of 150 mg (0.35 mmol) of 2'-[(t-butoxycarbonylamino)methyl]-4-[(t-butyldimethylsiloxy)-methyl]-1,1'-biphenyl (Step G) in 2 mL of dry tetrahydrofuran under a nitrogen atmosphere was added by syringe 0.52 mL (0.53 mmol) of 1.0M solution of tetra-n-butylammonium fluoride in tetrahydrofuran. The reaction mixture was stirred for one hour then diluted with 100 mL of ethyl acetate. The mixture was washed with water (3×20 mL), then saturated aqueous sodium chloride, dried over magnesium sulfate and filtered. The solvent was removed under vacuum to give an oil which was purified by column chromatography on silica gel eluting with hexanes/ethyl acetate (55:45) to afford 101 mg (93%) of the product as a white solid. FAB-MS: calculated for C19H23NO3 313; found 314 (M+H). 1H NMR (200 MHz, CDCl3): 1.40 (s, 9H), 2.50 (s, 2H), 4.20 (s, 2H), 4.70 (s, 2H), 7.18-7.45 (s, 8H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05583130
출처 데이터셋uspto-grants-1996_12
ORD IDord-36a9228dd73b4ffbb152b500429a6256
출처 메모uspto-grants-1996_12