Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643693Generated: November 1, 2026

Imidazole → 3,5-Bis(methoxymethoxy)benzyl tert-butyldimethylsilyl ether

https://huagongshe.com/reaction/1643693

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant3,5-Bis(methoxymethoxy)benzylalcoholHCID 10443751—
SolventDichloromethaneHCID 6344—
Product3,5-Bis(methoxymethoxy)benzyl tert-butyldimethylsilyl etherHCID 999751697%

Reaction Steps

To a solution of (3,5-bis-methoxymethoxy-phenyl)-methanol (220b) (290 g, 1.27 mol) and imidazole (129 g, 1.9 mol) in CH2Cl2 (1.5 L) was added TBSCl (286 g, 1.9 mol) at 5° C. in several portion was stirred at room temperature overnight. TLC (EtOAc/petroleum ether=1/2) showed that the reaction was complete. The mixture was filtered and the filtrate was washed with water, dried over Na2SO4 and concentrated under high vacuum to give the title compound (320 g, 97%) as a brown oil. 1H NMR (400 MHz, CDCl3): δ 6.68 (d, 2H), 6.57(t, 1H), 5.14 (s, 4H), 4.66 (s, 2H), 3.48 (s, 6H), 0.94 (s, 9H), 0.07 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119624B2
Source datasetuspto-grants-2012_02
ORD IDord-59ce6d2eb24144e89682b294515394be
Source noteuspto-grants-2012_02