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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1372548생성일: 2026년 10월 27일

1,3-Bis(4-nitrophenoxy)-2,2-bis[(4-nitrophenoxy)methyl]propane → 4,4'-((2,2-Bis((4-aminophenoxy)methyl)propane-1,3-diyl)bis(oxy))dianiline

https://huagongshe.com/reaction/1372548

반응식

참여 물질

역할이름HCID투입량
반응물1,3-Bis(4-nitrophenoxy)-2,2-bis[(4-nitrophenoxy)methyl]propaneHCID 12104991—
반응물HCID 178418361HCID 178418361—
촉매PalladiumHCID 23938—
용매TetrahydrofuranHCID 8028—
생성물4,4'-((2,2-Bis((4-aminophenoxy)methyl)propane-1,3-diyl)bis(oxy))dianilineHCID 2201543090%

반응 단계

A mixture of 1,3-bis(4-nitrophenoxy)-2,2-bis[(4-nitrophenoxy)methyl]propane (15.43 grams, 24.87 mmol; prepared as described in Part B of this Example) and Pd/C 10% (1.58 grams, obtained from Aldrich Chemical Co.) was stirred for 70 hours in tetrahydrofuran (400 milliliters) under 180 pounds per square inch of hydrogen gas. The mixture was then filtered over CELITE, and the solvent was removed by evaporation under reduced pressure. The residue was recrystallized from nitrobenzene/benzene to afford pure 1,3-bis(4-aminophenoxy)-2,2-bis[(4-aminophenoxy)methyl]propane (11.17 grams, 22.31 mmol, 90 percent yield) as small light brown crystals: mp 210–211° C.; IR (KBr) 3434, 3351, 3050, 2932, 1625, 1511, 1467, 1232, 1041, 1172, 831, 523 cm−1; 1H NMR (400 MHz, DMSO-d6) δ 6.66 (d, 8H, 3J=8.4 Hz), 6.47 (d, 8H, 3J=8.4 Hz), 4.62 (s, 8H), 4.03 (s, 8H); 13C NMR (100 MHz, DMSO-d6) δ 150.14, 142.73, 115.76, 114.86, 67.06, 44.59; MS (FAB, 3-nitrobenzyl alcohol) m/e 500.3; Anal. Calcd for C33H24N4O4: C, 69.58; H, 6.44; N, 11.19. Found: C, 69.33; H, 6.78; N, 10.91.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07157601B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-e913d8d04c074da8af18f478d013a992
출처 메모uspto-grants-2007_01