(CAS NO.: ), with other names as Ketone, 2-fluorenyl methyl, could be produced through the following synthetic routes.

A 1-l. three-necked round-bottomed flask is fitted with a dropping funnel, a reflux condenser attached to a hydrogen chloride absorption trap,1 and a very sturdy mechanical stirrer, which may be of the mercury-sealed or rubber-sleeve type. In the flask are placed 350 ml. of dry disulfide and 80 g. (0.48 mole) of fluorene. The stirrer is started, and, after the fluorene has dissolved, 128 g. (0.96 mole) of anhydrous aluminum chloride is added in one portion. In the dropping funnel is placed 49.4 g. (0.48 mole) of redistilled acetic anhydride, and about 1 ml. of it is added dropwise to the vigorously stirred dark red reaction mixture. If the reaction does not start immediately it is initiated by warming the reaction flask in a water bath. After the reaction has started, the balance of the acetic anhydride is added at such a rate that the carbon disulfide refluxes gently; about 45–55 minutes is required. When approximately one-half of the acetic anhydride has been added an addition complex separates as a heavy mass which makes stirring very difficult. However, stirring must be maintained to prevent excessive local reaction at the point of introduction of the acetic anhydride. The mixture is stirred and refluxed on the water bath for an hour after the addition of the acetic anhydride is complete.

The dark green mass is collected on a large Büchner funnel and transferred as quickly as possible to a 1-l. beaker in which it is stirred mechanically for 10 minutes with 300 ml. of carbon disulfide. The solid is again collected and washed on the filter with two 50-ml. portions of carbon disulfide and with one 100-ml. portion of petroleum ether (b.p. 28–35°). The resulting granular aluminum chloride complex is decomposed by portionwise addition to a well-stirred mixture of 800 ml. of water and 30 ml. of concentrated hydrochloric acid in a 2-l. beaker under a hood. Each portion is allowed to hydrolyze before the next is added. The hydrolysis mixture should not be cooled. The crude 2-acetylfluorene is collected on a filter and washed three times with 100-ml. portions of water. After drying in an oven at 100° for 3 hours the light-orange ketone weighs 83–95 g. (83–95%) and melts over the range 113–117°. This crude product is transferred to a 2-l. round-bottomed flask containing 800 ml. of 95% ethanol and 5 g. of decolorizing carbon. The mixture is refluxed for 1 hour and filtered hot. On cooling the filtrate deposits 71–83 g. of light-tan solid melting at 120–123°. A second recrystallization from 800 ml. of ethanol yields 55–63 g. (55–63%) of a light-cream-colored powder which melts at 124–126° and which is pure enough for most purposes.

Notice: Carbon disulfide, used as a solvent in this preparation, is highly inflammable; its vapor may ignite on contact with a hot laboratory steam line.