Hydrogen Bromide → 2-Bromo-1-(5-methyloxolan-2-yl)ethan-1-one

Participants

Reaction Steps

A solution of 5-methyl-2-tetrahydrofuroic acid (1.80 g, 13.85 mmol) in dichloromethane (25 ml) was treated with oxalyl chloride (2.4 ml, 27.51 mmol) in the presence of dimethylformamide (3 drops). After stirring for 1.25 h, the solvent was evaporated in vacuo. The residue was redissolved in dichloromethane and concentrated again. Excess diazomethane was then bubbled through a solution of the resulting acid chloride in dichloromethane (30 ml) at 0° C. When the addition was complete, the mixture was stirred for 10 min. at 0° C. and then treated with 48% aqueous hydrogen bromide (2.6 ml, 15.41 mmol). The mixture was stirred for 15 min. at room temperature, washed with water (×2), dried and concentrated in vacuo to yield the crude title compound as a brown oil (1.67 g, 58%); νmax (CH2Cl2) 1735, 1387 and 1086 cm-1 ; δH (CDCl3, 90 MHz) 1.33 (3H, d, J 6.0 Hz), 1.48 (1H, m), 1.90-2.35 (3H, m), 4.10 (1H, m), 4.25 (2H, s) and 4.48 (1H, m).

Provenance & Evidence