Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235083Generated: October 25, 2026

Water → 5-Ethyl-2-thiophenecarboxylic acid, N-t-butyl amide

https://huagongshe.com/reaction/235083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTert-ButylamineHCID 6385—
ReactantThionyl ChlorideHCID 24386—
Reactant5-Ethylthiophene-2-carboxylic acidHCID 588192—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
Product5-Ethyl-2-thiophenecarboxylic acid, N-t-butyl amideHCID 6069932480%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 28 g (0.18 mol) of 5-ethyl-2-thiophenecarboxylic acid, from step 3a above, in 130 mL of methylene chloride was added a large excess (130 mL, 10 mol) of thionyl chloride, and the solution was heated at reflux for 2 hours. The solvent and excess reagent were removed by evaporation, and the residue was dissolved in 130 mL of chloroform and cooled to 0° C. To this solution was added 94 mL (0.9 mol) of t-butylamine dropwise, and the solution was stirred at reflux for 2 hours. The reaction was cooled, the solution poured into water, and the mixture extracted with ethyl acetate. The extract was washed with water and brine, dried, and concentrated. The residue was dissolved in ethyl acetate and the crude product was precipitated by addition of hexane. The crude product was collected by filtration and purified by flash chromatography over silica gel, eluting with 1:6 ethyl acetate:hexane, to afford 13.3 g (80% yield) of the title product after drying. MS 212 (M+H)+. NMR (CDCl3) δ: 7.25 (d, 1H, J=3 Hz), 6,72 (d, 1H, J=3 Hz), 5.70 (bs, 1H), 2.84 (q, 2H, J=7 Hz), 1.45 (s, 9H), 1.31 (t, 3H, J=7 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05597832
Source datasetuspto-grants-1997_01
ORD IDord-23b6fc38c21d44bf962b28e9020bf8fb
Source noteuspto-grants-1997_01