Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734435Generated: October 30, 2026

Triethylamine → 6-[3-(Tert-butyl-dimethyl-silanyloxy)-propoxy]-nicotinonitrile

https://huagongshe.com/reaction/734435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant6-(3-Hydroxypropoxy)nicotinonitrileHCID 43152139—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
Product6-[3-(Tert-butyl-dimethyl-silanyloxy)-propoxy]-nicotinonitrileHCID 5784543169.5%

Reaction Steps

To a solution of t-butyldimethylsilyl chloride (0.93 g, 6.17 mmol) in CH2Cl2 (25 mL) was added 6-(3-hydroxypropoxy)nicotinonitrile (Example 66, 1 g, 5.61 mmol), Et3N (0.62 g, 6.17 mmol), and DMAP (0.014 g, 0.11 mmol). The mixture was stirred at rt for 18 h. The reaction mixture was diluted with brine and extracted with CH2Cl2 (3×25 mL). The combined organic layers were dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude residue was purified by silica gel flash chromatography (2:1 hexanes/EtOAc) to give the title compound (1.14 g, 69%). 1H NMR (400 MHz, CDCl3) δ 8.40 (dd, 1H), 7.69 (dd, 1H), 6.72 (dd, 1H), 4.40 (t, 2H), 3.73 (t, 2H), 1.90-1.98 (m, 2H), 0.82 (s, 9H), 0.02 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592361B2
Source datasetuspto-grants-2009_09
ORD IDord-c52599b7f28e4e838799b88875c3af98
Source noteuspto-grants-2009_09