HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871124Generated: October 26, 2026
3-Bromo-2-fluorobenzaldehyde → (3-Bromo-2-fluorophenyl)(phenyl)methanol
https://huagongshe.com/reaction/871124
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Bromo-2-fluorobenzaldehyde | HCID 22019361 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Bromo-2-fluorophenyl)(phenyl)methanol | HCID 71743205 | — |
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 phenylmagnesium bromide (0.887 mL, 0.887 mmol). The reaction mixture was maintained at −78° C. for at least 1 hr and then allowed to warm to room temperature slowly over 3 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 twice with CH2Cl2. The organic layers were combined, dried over Na2SO4, filtered, and concentrated to afford the title compound as a colorless 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-cdc94b3ba03c4bd78911e3a632065075 |
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| Source note | uspto-grants-2015_03 |
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