α-Chlorophenyl (CAS no.: ), which is also known as Acetic acid, chlorophenyl-, could be produced through the following synthetic routes.

A. Ethyl mandelate. To 152 g. (1.0 mole) of mandelic acid and 200 ml. of absolute ethanol in a 1-l. round-bottomed flask equipped with a reflux condenser, there is added 100 ml. of absolute ethanol containing about 10 g. of anhydrous hydrogen chloride. The solution is heated under reflux on a steam bath for 5 hours, then poured into 1 l. of ice water in a 3-l. beaker. A saturated aqueous solution of sodium bicarbonate is added until the mixture is faintly alkaline. It is then extracted with two 300-ml. portions of ether in a 2-l. separatory funnel. The ether extracts are washed with a 200-ml. portion of water and dried over 50 g. of anhydrous sodium sulfate. The dried ether solution is concentrated by distillation from a 250-ml. Claisen flask, and the residue is distilled at reduced pressure. There is obtained 147–154 g. (82–86%) of ethyl mandelate, b.p. 144–145°/16 mm. The ester may crystallize upon standing for a prolonged period. It melts at 30.5–31.5°.

B. Ethyl α-chlorophenylacetate. Ethyl mandelate (135 g., 0.75 mole) is dissolved in 98 g. (59 ml., 0.82 mole) of chloride contained in a 500-ml. round-bottomed flask equipped with a reflux condenser capped with a drying tube. The apparatus is allowed to stand in a hood overnight (about 16 hours), at the end of which time the solution is heated under reflux for 30 minutes on a steam bath. The solution is then poured into 750 ml. of ice water contained in a 2-l. separatory funnel, and the mixture is extracted with two 300-ml. portions of ether. The combined ether extracts are washed with two 250-ml. portions of saturated aqueous sodium bicarbonate solution and one 250-ml. portion of water. The washed extracts are dried over 45 g. of anhydrous sodium sulfate and concentrated by distillation. The residue is distilled from a 250-ml. Claisen flask at reduced pressure. The yield of ethyl α-chlorophenylacetate is 121–127 g. (81–85%), b.p. 134–136°/15 mm., n_D²⁰ 1.5149.

C. α-Chlorophenylacetic acid. A solution of 119 g. (0.6 mole) of ethyl α-chlorophenylacetate in 238 ml. of glacial acetic acid and 119 ml. of concentrated hydrochloric acid, contained in a 1-l. round-bottomed flask, is heated under reflux in a hood for 1.5 hours. At the end of the heating period the solution is concentrated by heating in an oil bath at 100° at reduced pressure (15–20 mm.) until no further material is distilled. The residue is allowed to cool to room temperature and poured slowly, with stirring, into 1-l. of ice-cold saturated sodium bicarbonate solution contained in a 2-l. beaker. Solid sodium bicarbonate is added in small portions until the solution becomes neutral to universal indicator paper. The solution is then extracted with two 200-ml. portions of ether in a 2-l. separatory funnel. The aqueous phase is placed in a 3-l. beaker and acidified cautiously with ice-cold 12N sulfuric acid until the mixture is acid to paper. The oily suspension is extracted with two 200-ml. portions of ether in a 2-l. separatory funnel. The ether extracts are washed with two 100-ml. portions of water and dried over 45 g. of anhydrous sodium sulfate. The dried ether extract is transferred to a 1-l. Erlenmeyer flask and concentrated on a steam bath until ether is no longer distilled. To the residue there is added 500 ml. of warm (50–60°) concentrated hydrochloric acid (in a hood), and the suspension is allowed to cool with occasional swirling. Crystallization is completed by chilling in ice, and the product is collected on a sintered-glass funnel. After the product has been dried as much as possible on the funnel it is dried to constant weight in a vacuum desiccator over solid potassium hydroxide. The yield of dry acid is 82–84 g. (80–82%), m.p. 77.5–79.5°. It is satisfactory for most purposes. If very pure material is desired the acid may be recrystallized from three volumes of hexane to give material, m.p. 78.5–79.5°, in 90–95% recovery.