Iodine → 4-Methyl-1-thiophen-3-yl-pentan-1-one

Magnesium powder (1.49 g, 61.3 mmol) was added to dry diethyl ether (100 ml) under nitrogen atmosphere. One iodine crystal (catalytic) was added, followed by 1-bromo-3-methylbutane (6.3 ml, 52.6 mmol). The reaction was initiated by sonication at 30° C. and was allowed to spontaneously reflux. Once the exothermic reaction had subsided, the mixture was added by cannulation to a solution of thiophene-3-carboxylic acid methoxy-methyl-amide (7.50 g, 43.8 mmol) in dry diethyl ether (10 ml). Once addition was complete, the mixture was stirred at room temperature for 2 hours. The reaction mixture was then washed with saturated ammonium chloride (2×150 ml), dried (Na2SO4) and concentrated in vacuo. The crude yellow oil was purified by silica gel chromatography to yield the title compound as a colourless oil (1.55 g, 19%). 8H (d6 DMSO): 0.88 (6H, d), 1.49 (2H, q), 1.56 (1H, m), 2.90 (2H, t), 7.49 (1H, d), 7.59 (1H, d), 8.50 (1H, s).

1. customThe reaction was initiated by sonication at 30° C.
2. temperatureto spontaneously reflux
3. customOnce the exothermic reaction
4. additionOnce addition
5. washThe reaction mixture was then washed with saturated ammonium chloride (2×150 ml)
6. dry with materialdried (Na2SO4)
7. concentrationconcentrated in vacuo
8. customThe crude yellow oil was purified by silica gel chromatography

ORD record

ord-e675861364dc48248337434582ad7eb1

Source dataset

uspto-grants-2011_09

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08017619B2