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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1089256생성일: 2026년 10월 26일

Sodium Chloride → 1,4-Bis(4-methoxybenzyloxy)butan-2-ol

https://huagongshe.com/reaction/1089256

반응식

참여 물질

역할이름HCID투입량
반응물Sodium ChlorideHCID 5234—
반응물Sodium HydroxideHCID 14798—
반응물Sodium borohydrideHCID 4311764—
반응물1,4-Bis(4-methoxybenzyloxy)but-2-eneHCID 54555137—
촉매Mercury bis(trifluoroacetate)HCID 2723924—
용매TetrahydrofuranHCID 8028—
생성물1,4-Bis(4-methoxybenzyloxy)butan-2-olHCID 1481421391%

반응 단계

To a solution of mercury (II) trifluoroacetate (17.1 g, 40 ml) in aqueous tetrahydrofuran (1:1, 80 ml) was added a solution of 1,4-bis(4-methoxybenzyloxy)but-2-ene (12.8 g, 39 mmol) in tetrahydrofuran (10 ml) over 5 minutes. The resulting 2-phase mixture was stirred vigorously at room temperature for 15 minutes. To the mixture was added aqueous sodium hydroxide (40 ml, 3M) followed by sodium borohydride (0.5M solution in 3M sodium hydroxide; 40 ml) with water-bath cooling. The solution was saturated with sodium chloride and allowed to stand. The organic layer was collected, dried (magnesium sulphate) and filtered through celite. The solvent was removed to afford 1,4-bis(4-methoxybenzyloxy)butan-2-ol (12.27 g, 91%), IR: υmax (KBr) 3440, 2940, 2860, 1610, 1510 and 1250 cm-1 ; 1H NMR: δH (CDCl3) 1.76 (2H, q, J=6.0 Hz, 3-H), 2.90 (1H, br, D2O exchangeable, OH), 3.41 (2H, AB of ABX JAX =6.9 Hz, JBX =4.2 Hz and JAB =9.5 Hz, 1-H), 3.62 (2H, m, 4-H), 3.80 (6H, s, 2×CH3), 4.00 (1H, m, 2-H), 4.43 (2H, s, ArCH2), 4.48 (2H, s, ArCH2), 6.86 (4H, m, ArH) and 7.24 (4H, m, ArH).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04965270
출처 데이터셋uspto-grants-1990_10
ORD IDord-877aa27bbb244298bdf0934a84ff7f98
출처 메모uspto-grants-1990_10