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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1379849Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1379849

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsopropanolHCID 3776—
EduktSodium HydroxideHCID 14798—
Edukt2-Bromo-N-(tert-butoxycarbonyl)benzylamineHCID 7018300—
Edukt(4-(((tert-Butyldiphenylsilyl)oxy)methyl)phenyl)boronic acidHCID 15224568—
KatalysatorTetrakis(triphenylphosphine)palladiumHCID 11979704—
LösungsmittelBenzeneHCID 241—
LösungsmittelWaterHCID 962—
Produkt2'-[(t-Butoxycarbonylamino)methyl]-4-[(t-butyldiphenylsiloxy)methyl]-1,1'-biphenylHCID 22008454100%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05672596
Quelldatensatzuspto-grants-1997_09
ORD IDord-a04fa0c255334a9a8bf435bca4ca3519
Quellennotizuspto-grants-1997_09