HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871125Generated: October 30, 2026
3-Bromo-2-fluorobenzaldehyde → (3-Bromo-2-fluorophenyl)(4-fluorophenyl)methanol
https://huagongshe.com/reaction/871125
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromo-2-fluorobenzaldehyde | HCID 22019361 | — |
| Reactant | HCID 178418676 | HCID 178418676 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Bromo-2-fluorophenyl)(4-fluorophenyl)methanol | HCID 86730390 | — |
Reaction Steps
To a solution of 3-bromo-2-fluorobenzaldehyde (0.150 g, 0.739 mmol) in THF (3.21 mL) cooled to −78° C. was added (4-fluorophenyl)magnesium bromide (0.443 mL, 0.887 mmol). The reaction mixture was maintained at −78° C. for at least 1 hr, then allowed to warm to room temperature slowly over 2 hr. The reaction was quenched with a saturated aqueous solution of NH4Cl. The reaction mixture was diluted with CH2Cl2 and the layers were separated. The aqueous phase was extracted with CH2Cl2 (2×). Organics were combined, dried over Na2SO4, filtered, and concentrated to afford the title compound as a yellow residue.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969586B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-58e492eb32b1484eb7c606e467ec7abc |
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| Source note | uspto-grants-2015_03 |
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