HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015635Generated: October 31, 2026
Isobutylene → 3-tert-Butylamino-5-phenyl-thiophene-2-carboxylic acid methyl ester
https://huagongshe.com/reaction/1015635
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isobutylene | HCID 8255 | — |
| Reactant | Methyl 3-amino-5-phenylthiophene-2-carboxylate | HCID 700562 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Solvent | Dioxane chloroform | HCID 66618785 | — |
| Product | 3-tert-Butylamino-5-phenyl-thiophene-2-carboxylic acid methyl ester | HCID 20775771 | 62% |
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/chloroforme (2:3) in a sealed tube. After cooling the solution at −78° C., put 20 ml of isobutene gaz. The sealed tube was closed and then the reaction mixture was stirred for 6 days at 60° C. The solvant 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07985769B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-a36a346359664772944241a1570c0ce2 |
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| Source note | uspto-grants-2011_07 |
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