HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549424Generated: October 27, 2026
t-Butyl bromide → Tert-butyl 4-cyano-5-(methylthio)thiophene-2-carboxylate
https://huagongshe.com/reaction/549424
Participants
| Role | Name | HCID | Charge |
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| Reactant | t-Butyl bromide | HCID 10485 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Cyano-5-methylsulfanylthiophene-2-carboxylic acid | HCID 45594312 | — |
| Catalyst | Benzyltrimethylammonium chloride | HCID 5963 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | Tert-butyl 4-cyano-5-(methylthio)thiophene-2-carboxylate | HCID 66785900 | 58.7% |
Reaction Steps
A mixture of 4-cyano-5-(methylthio)thiophene-2-carboxylic acid (2.0 g, 10 mmol), benzyltrimethylamonium chloride (2.25 g, 10 mmol), tertbutyl bromide (54 mL, 480 mmol) and anhydrous potassium carbonate (36 g, 260 mmol) in dimethylacetamide (100 mL) was stirred at 60° C. for 6 hours. After cooling, the mixture was diluted with ethyl acetate (400 mL) and washed with water. Organic layer was dried and evaporated under reduced pressure to give a residue which was purified by chromatography (eluent ethyl acetate/n-hexane 3:1) thus yielding 1.5 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07943654B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-cf4a26b45de24e88ad0104e71e6be0cb |
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| Source note | uspto-grants-2011_05 |
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