2-Methylbenzyldimethylamine (CAS NO.: 4525-48-8), which is also known as , N,N,o-trimethyl-, could be produced through the following synthesis routes.

A. Benzyltrimethyl. A solution of 135 g. (1 mole) of N,N-dimethylbenzylamine in 200 ml. of commercial absolute ethanol is placed in a three-necked flask fitted with a 125-ml. dropping funnel, a reflux condenser, and a rubber slip-sleeve-sealed stirrer. The openings of the dropping funnel and condenser are protected from atmospheric moisture with drying tubes. While the solution is stirred rapidly, 190 g. (1.34 moles) of methyl iodide contained in the dropping funnel is added slowly at first, then at such a rate as to cause gentle refluxing of the solution. After the addition is complete (30 minutes), the solution is boiled under reflux on the steam bath for 30 minutes more and transferred to a 2-l. Erlenmeyer flask with the aid of an additional 25-ml. of absolute ethanol for rinsing. On cooling to room temperature a large portion of the methiodide crystallizes, and the remaining material is then precipitated by the addition of 1 l. of anhydrous ether with stirring. The product is separated by suction filtration, washed with two 100-ml. portions of anhydrous ether, and dried in air at room temperature. The yield of benzyltrimethylammonium iodide, m.p. 178–179° (dec.), is 260–274 g. (94–99%), and is pure enough for most purposes.

B. 2-Methylbenzyldimethylamine (CAS NO.: 4525-48-8). (Caution! This preparation should be conducted in a good hood to avoid exposure to ammonia). To 800 ml. of liquid ammonia contained in a 2-l. three-necked flask fitted with a rubber slip-sleeve-sealed wire stirrer and an air-cooled reflux condenser, sodium is added in small pieces until the blue color persists. At this point 0.5 g. of granulated ferric nitrate is added, and then 27.8 g. (1.2 g. atoms) of sodium (cut into approximately 0.5-g. pieces), is introduced at such a rate that stirring is not hindered. After all the sodium has been added (about 15 minutes), the mixture is stirred until the blue color disappears and the grayish-black suspension of sodium amide remains (15–20 minutes). Stirring is discontinued, and the mixture is swirled to wash down the mirror of sodium which forms on the upper walls of the flask.

A 500-ml. Erlenmeyer flask is charged with 277 g. (1 mole) of benzyltrimethylammonium iodide (prepared as described in Part A) and is connected with a short section of large-diameter rubber tubing to the third neck of the flask containing the sodium amide. Stirring is started, and the salt is shaken in at a steady rate and as rapidly as possible without serious loss of material through the condenser. This operation requires about 10–15 minutes. The greenish-violet color, which is first produced by addition of the salt, persists for about 15 minutes after all the material has been added. During this and the subsequent reaction period, more ammonia is added as necessary to maintain the original volume. The mixture is stirred for an additional 2 hours, and then 27 g. (0.5 mole) of ammonium chloride is added cautiously to destroy excess sodium amide.

The flask is fitted with a dropping funnel, and enough (about 100 ml.) water is added, dropwise at first, to bring all the solid material into solution. The mixture is stirred until it reaches room temperature, 70 ml. of ether is added, and the organic layer is separated. The water layer is extracted with two 70-ml. portions of ether, and the combined ether solutions are washed with two 50-ml. portions of saturated salt solution and dried over anhydrous potassium carbonate. After filtration and removal of the ether by distillation, the amine is distilled through a 10-cm. Vigreux column. The fraction, b.p. 72–73°/9 mm.., 97–99°/13 mm., or 197–198°/atm., amounts to 134–141.5 g. (90–95% yield), n_D20 1.5050–1.5060. On redistillation all but about 5% of the material is recovered, b.p. 78–79°/12 mm., n_D20 1.5049–1.5052.