(CAS no.: ), which is also known as Cyanotrimethylsilane, could be produced through the following synthetic routes.

A. Trimethylsilyl cyanide. A 1-L, round-bottomed flask equipped with a magnetic stirrer, nitrogen inlet, and a 60-mL addition funnel is charged with 5.0 g (0.624 mol) of lithium hydride and 500 mL of anhydrous tetrahydrofuran. The stirred suspension is cooled in an ice bath and 42.6 g of acetone cyanohydrin (45.7 mL, 0.501 mol) is added dropwise over 15 min. After the addition is complete, the ice bath is removed and the mixture stirred for 2 hr at room temperature. The magnetic stirring bar is removed and the solvent evaporated as completely as possible on a rotary evaporator. The white lithium cyanide is then dried in vacuo for 3 hr. The lithium cyanide is freed from the sides of the flask and broken up with a spatula. A 250-mL round-bottomed flask equipped with an ice bath, magnetic stirrer, thermometer, and nitrogen inlet is charged with 54.32 g (63.46 ml, 0.500 mol) of and 100 mL of bis[2-(2-methoxyethoxy)ethyl] ether. The lithium cyanide is added to this stirred solution over 15 min through Gooch tubing. After the addition is complete, the ice bath is removed and the milky suspension stirred overnight at room temperature. The Gooch tubing and the thermometer are then removed from the reaction flask and a stillhead equipped for downward vacuum distillation is attached. A 100-mL, round-bottomed flask immersed halfway in an acetone-dry ice slush bath is employed as the receiver. The volatile compounds are distilled under a pressure of 50 mm (bp 25–55°C) by heating the contents of the pot using an oil bath. The distillate is carefully redistilled through a well-insulated 15-cm column packed with glass helices under an inert atmosphere. A 25–40 mL forerun (bp 66–113°C), consisting primarily of tetrahydrofuran and hexamethyldisiloxane, is first collected. The second fraction, containing 29–41 g (59–82%) of trimethylsilyl cyanide, bp 114–117°C, n_D²⁵ 1.3902, then distills. A purity of ca. 97% was established by GC analysis; the product is suitable for synthetic use without further purification.

B. Cyanosilylation of . A 100-mL, round-bottomed flask equipped with a magnetic stirrer, West condenser, and a nitrogen inlet is charged with 6.30 g (58.2 mmol) of p-benzoquinone, 10 mL of dry carbon tetrachloride, and 8 mL (63.03 mmol) of trimethylsilyl cyanide. The stirred suspension is heated to a gentle reflux by means of a heat gun to dissolve all the p-benzoquinone. It is then allowed to cool slowly until the crystallization of the p-benzoquinone starts, at which time 5 mg of the 1 : 1 complex between potassium cyanide and 18-crown-6 is added through the top of the condenser. An immediate vigorous reflux sets in and continues for 1–2 min. The stirred reaction mixture is permitted to cool slowly to room temperature, whereupon the condenser is removed and 3 g of Florisil is added. After stirring for an additional 15 min, 10 mL of dry carbon tetrachloride is added. The suspension is then filtered and the filtercake leached with three 5-mL portions of carbon tetrachloride. The solvent is evaporated from the filtrate as completely as possible on a rotary evaporator, at which point crystallization of the residue usually begins. The last traces of solvent and trimethylsilyl cyanide are then removed in vacuo over 20 hr at 50 μ to afford 12.0–12.2 g of crude product. The trimethylsilyl cyanohydrin is recrystallized by dissolving the crude material in 25 mL of hot hexane and allowing the resulting solution to cool slowly to room temperature. After collection by filtration the product is rinsed with two 5-mL portions of hexane and airdried to yield 7.54–9.77 g (63%–81%) of white to buff-colored needles, mp 65–67°C.