Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromothiophene | HCID 13851 | — |
| Reactant | 4-Heptanone | HCID 31246 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66609090 | HCID 66609090 | — |
Reaction Steps
A solution of 2-bromothiophene (10.0 g, 61.5 mmol) in dry THF (60 mL) was cooled to −78° C. under nitrogen. A solution of n-BuLi (2.5 M, 27.0 mL, 67.5 mmol) was then added slowly, and the resulting mixture was stirred at −78° C. for 2 hours, before a solution of 4-heptanone (8.5 g, 74.4 mmol) in dry THF (10 mL) was added slowly. This mixture was stirred at −78° C. for an additional 1 hour, and then allowed to warm to room temperature, and stirred at room temperature overnight. Most of the solvent was removed in vacuo, and the residue was subjected to flash column chromatography on silica gel with a hexane:EtOAc (3:1, v/v) mixture, leading to a colorless oil as the product (10.2 g, 83.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598575B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-9640c1b4ed984adfb4657f475a4649ef |
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| Source note | uspto-grants-2013_12 |
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