HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57458Generated: October 26, 2026
4-Bromo-3-fluorobenzaldehyde → 1-(4-Bromo-3-fluorophenyl)ethan-1-ol
https://huagongshe.com/reaction/57458
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromo-3-fluorobenzaldehyde | HCID 2783411 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(4-Bromo-3-fluorophenyl)ethan-1-ol | HCID 71756542 | — |
Reaction Steps
Methylmagnesium bromide (3M in diethylether, 6.77 mL, 20.31 mmol) was added dropwise over ˜15 min to a solution of 4-bromo-3-fluorobenzaldehyde (3.1 g, 15.27 mmol) in THF (50 mL) under argon at a temperature of −60° C. to −50° C. The ice bath was removed and the reaction mixture was allowed to warm to room temperature and stirred ˜20 hr. The reaction mixture was slowly diluted/quenched with saturated aqueous ammonium chloride solution (20 mL) and further diluted with water (10 mL). The separated aqueous layer was extracted with ethyl acetate (2×40 mL). The combined organic layers were washed with brine (60 mL), dried over sodium sulfate, filtered and concentrated under reduced pressure to provide crude 1-(4-bromo-3-fluorophenyl)ethanol as a pale yellow oil, which was directly used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434719B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-7c6b01ce93e14c73ba9a5c6e4f2dc85a |
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| Source note | uspto-grants-2016_09 |
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