HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406270Generated: October 30, 2026
2-Bromo-5-fluorobenzaldehyde → HCID 58140257, compound
https://huagongshe.com/reaction/1406270
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromo-5-fluorobenzaldehyde | HCID 2773321 | — |
| Reactant | HCID 178418332 | HCID 178418332 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58140257 | HCID 58140257 | 75.3% |
Reaction Steps
To a solution of 2-bromo-5-fluoro-benzaldehyde (17.0 g, 83.7 mmol) in tetrahydrofuran (100 mL), cooled to 0° C. under nitrogen, was added methyl magnesium chloride solution (3M in tetrahydrofuran, 31.0 mL, 93.0 mmol, 1.1 eq.) dropwise over a 20 min period. The resulting solution was stirred at 0° C. for 45 min before quenching with aqueous ammonium chloride solution (1M, 17 mL). The resulting mixture was partitioned between pentane (300 mL) and water (100 mL). The organic phase was washed with brine (50 mL) and then dried over magnesium sulphate. This mixture was filtered and concentrated under reduced pressure. The residue was purified by chromatography on silica gel eluting with a gradient of toluene in pentane (50:50 to 100:0 by volume) to produce the title compound as a colourless oil (13.8 g, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916593B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-60d25aaef0ac470b8a8a73fa7b27693f |
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| Source note | uspto-grants-2014_12 |
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