HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221917Generated: October 25, 2026
Dimethylformamide → 5-Bromo-2-fluoro-4-(hydroxymethyl)benzaldehyde
https://huagongshe.com/reaction/221917
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2-Bromo-5-fluorobenzyl alcohol | HCID 2773349 | — |
| Reactant | 1,2,2,3-Tetramethylpiperidine | HCID 18761772 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Bromo-2-fluoro-4-(hydroxymethyl)benzaldehyde | HCID 59278930 | 106.7% |
Reaction Steps
Tetramethylpiperidine (0.68 g, 4.87 mmol) was dissolved in tetrahydrofuran (4.5 mL). To the resultant solution was added n-butyllithium (1.0 M n-hexane solution, 4.88 mL) at 0° C., and the solution was then stirred for 15 minutes. The solution was cooled to −78° C., and a solution of (2-bromo-5-fluorophenyl)-methanol (0.50 g, 2.43 mmol) in tetrahydrofuran (2.5 mL) was added dropwise. The temperature of the solution was raised over 2 hours to −40° C. The solution was again cooled to −78° C., and N,N-dimethylformamide (0.47 mL, 6.07 mmol) was added thereto. The temperature of the solution was raised to room temperature, and the solution was then stirred for 30 minutes. Saturated aqueous ammonium chloride was added, and the resultant mixture was extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate, and then concentrated under reduced pressure, to thereby obtain the titled compound (604.3 mg, quantitative).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08207134B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-f40641d84fb74929ad904fe03f5c0e41 |
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| Source note | uspto-grants-2012_06 |
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