n-Butyl glyoxylate (CAS NO.: ), with other names as , n-butyl ester, could be produced through the following synthetic routes.

In a 3-l. three-necked round-bottomed flask provided with a Hershberg stirrer and a thermometer are placed 1.25 l. of reagent-grade benzene and 325 g. (1.24 moles) of di-n-butyl d-tartrate. The mixture is stirred rapidly, and 578 g. (1.30 moles) of lead tetraacetate is added over a period of about 25 minutes. The temperature is maintained below 30° by occasional cooling with cold water. After the addition is complete, the mixture is stirred for 1 hour, during which time the gummy salts become crystalline. The salts are removed by filtration with suction and washed with 500 ml. of benzene. The benzene and acetic acid are removed from the filtrate by distillation at 65°/50 mm. The residue is distilled at 20 mm. under nitrogen introduced through an ebullator, using a Vigreux column (2 by 30 cm.), and the fraction boiling between 65° and 79°/20 mm. (main portion at 68–74°) is collected as product. The crude n-butyl glyoxylate, which weighs 247–280 g. (77–87%), n²⁰D 1.442–1.443, d²⁵4 1.085, is satisfactory for most purposes.