HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850120Generated: November 2, 2026
Dimethylformamide → (S)-tert-butyl 1-(3-fluoro-4-formylphenyl)ethylcarbamate
https://huagongshe.com/reaction/1850120
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethylacetate heptane | HCID 21899848 | — |
| Reactant | (S)-tert-butyl 1-(4-bromo-3-fluorophenyl)ethylcarbamate | HCID 86730150 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-tert-butyl 1-(3-fluoro-4-formylphenyl)ethylcarbamate | HCID 86730149 | 26.2% |
Reaction Steps
A solution of (S)-tert-butyl 1-(4-bromo-3-fluorophenyl)ethylcarbamate (318 mg, 1 mmol) in dry THF (5 mL) was cooled to −78° C. BuLi (2.5 M, 840 μL, 2.1 mmol) was added dropwise and the resulting solution was stirred at −78° C. for 1 h. Then DMF (232 μL, 3.00 mmol) was added in one portion. The reaction was stirred for another 30 min at −78° C. then quenched with sat. NH4Cl solution. The reaction was stirred at room temperature for another 30 min then diluted with EtOAc, washed with water and brine. The separated organic was dried over Na2SO4, filtered and concentrated. Silica gel column chromatography (EtOAc/heptane 0 to 80%) provided (S)-tert-butyl 1-(3-fluoro-4-formylphenyl)ethylcarbamate as a white solid (70 mg, 26.2% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957068B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-7bc15e9c4bc544cd8e1e54dbea52e2e3 |
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| Source note | uspto-grants-2015_02 |
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