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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1089256Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1089256

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium ChlorideHCID 5234—
EduktSodium HydroxideHCID 14798—
EduktSodium borohydrideHCID 4311764—
Edukt1,4-Bis(4-methoxybenzyloxy)but-2-eneHCID 54555137—
KatalysatorMercury bis(trifluoroacetate)HCID 2723924—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1,4-Bis(4-methoxybenzyloxy)butan-2-olHCID 1481421391%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04965270
Quelldatensatzuspto-grants-1990_10
ORD IDord-877aa27bbb244298bdf0934a84ff7f98
Quellennotizuspto-grants-1990_10