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HRID 1879530作成日:2026年10月26日

Ethyl Acetate → Tert-butyl 4'-(benzyloxy)-2'-nitrobiphenyl-4-ylcarbamate

https://huagongshe.com/reaction/1879530

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Sodium CarbonateHCID 10340—
反応物tert-butyl N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]carbamateHCID 2734617—
反応物5-Benzyloxy-2-chloro-nitrobenzeneHCID 11043622—
触媒HCID 178418397HCID 178418397—
溶媒1,4-DioxaneHCID 31275—
生成物Tert-butyl 4'-(benzyloxy)-2'-nitrobiphenyl-4-ylcarbamateHCID 5816024688%

反応手順

To 4-(benzyloxy)-1-chloro-2-nitrobenzene (526 mg, 2 mmol) and tert-butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenylcarbamate (670 mg, 2.1 mmol) in 12 mL dioxane was added 4 mL of a 1 M Na2CO3 (aq) solution and Tetrakis(triphenylphosphine)palladium (69 mg, 0.06 mmol). The suspension was heated at reflux for 15 h under Ar atmosphere and cooled to rt. It was added EtOAc (100 mL) and washed with brine (80 mL), water (80 mL), and dried over MgSO4. After solvent removal, the residue was chromatographed (hexane/EtOAc) to afford tert-butyl 4′-(benzyloxy)-2′-nitrobiphenyl-4-ylcarbamate as a yellow solid (740 mg, 88%). 1H NMR (400 MHz, CDCl3) δ 7.44-7.34 (m, 8H), (d, J=8.4 Hz, 1H), 7.20-7.16 (m, 3H), 6.50 (s, 1H), 5.12 (s, 2H), 1.51 (s, 9H); MS (ESI) m/z 443 (M+Na+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08318132B2
出典データセットuspto-grants-2012_11
ORD IDord-4481982c35d04724826a0e195738e877
出典メモuspto-grants-2012_11