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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193919Generated: November 2, 2026

Isobutylene → 3-tert-Butylamino-5-phenyl-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/2193919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyleneHCID 8255—
ReactantMethyl 3-amino-5-phenylthiophene-2-carboxylateHCID 700562—
CatalystSulfuric AcidHCID 1118—
SolventDioxane chloroformHCID 66618785—
Product3-tert-Butylamino-5-phenyl-thiophene-2-carboxylic acid methyl esterHCID 2077577162%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Concentrated sulfuric acid (10 drop) was added to a solution of 3-Amino-5-phenyl-thiophene-2-carboxylic acid methyl ester (500 mg, 2.15 mmol) in 20 ml of dioxane/chloroform (2:3) in a sealed tube. After cooling the solution at −78° C., put 20 ml of isobutene gas. The sealed tube was closed and then the reaction mixture was stirred for 6 days at 60° C. The solvent was removed and then partitioned between 15 ml of sat. Na2CO3 solution and 15 ml of EtOAc. The organic layer was separated, the aqueous phase was washed twice with ethyl acetate and the combined ethyl acetate layer was dried (MgSO4), concentrated and the residue was purified by flash chromatography (5% EtOAc/Hexane) to obtain 385 mg (62%) of 3-tert-Butylamino-5-phenyl-thiophene-2-carboxylic acid methyl ester. NMR 1H (CDCl3, 400 MHz): 7.65 ppm (d, 2H, Haro); 7.44-7.38 ppm (m, 3H, Haro); 7.07 ppm (s, 1H, Haro); 3.86 ppm (s, 3H); 1.48 ppm (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329924B2
Source datasetuspto-grants-2012_12
ORD IDord-7e2547a8a47741248c84d8899ece356d
Source noteuspto-grants-2012_12