Hydrogen Bromide → HCID 15672517, compound

Participants

Reaction Steps

At 5° to 10° C., 225 g (1.46 mol) of cyclopropyl-2-thienylcarbinol was dripped over a period of 1 hour into 972ml of 48% strength hydrobromic acid. The mixture was kept for 2 hours at room temperature, after which the organic phase was separated off and the aqueous solution was extracted three times, each time with 300 ml of dichloromethane. The combined organic phases were washed neutral with dilute sodium hydroxide solution and water, dried over magnesium sulfate and evaporated down under reduced pressure. There was obtained 322 g (94%,corrected) of crude bromide (GC: 92%). 1H-NMR (250 MHZ, CDCl3): δ=2.65-2.80 (m, 2H), 3.46 (t,2H), 5.90-6.10 (m, 1H), 6.61 (d, 1H), 6.80-7.00 (m, 2H), 7.14 (d, 1H).

Provenance & Evidence