HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643342Generated: October 31, 2026
5-Bromo-2-fluorobenzaldehyde → 1-(5-Bromo-2-fluorophenyl)ethanol
https://huagongshe.com/reaction/643342
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Bromo-2-fluorobenzaldehyde | HCID 736327 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(5-Bromo-2-fluorophenyl)ethanol | HCID 44182055 | — |
Reaction Steps
To a solution of 5-bromo-2-fluorobenzaldehyde 101 (100 g, 0.492 mol) in ether (500 mL), cooled in an ice bath, was added a 3 M solution of methyl magnesium bromide in ether (173 mL, 0.516 mol) in a dropwise manner. The reaction mixture was stirred for 30 minutes in the ice bath. The reaction mixture was allowed to warm to room temperature and was stirred for 15 minutes. The reaction mixture was cooled in an ice bath and the reaction was quenched by addition of water in a dropwise manner. The reaction mixture was acidified with dilute hydrochloric acid. The organic layer was separated. The aqueous layer was extracted with ether for two times. The combined organic layer was dried over magnesium sulfate and evaporated under reduced pressure to afford 1-(5-Bromo-2-fluoro-phenyl)-ethanol 102 (106 g, 0.484 mol) which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700601B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-2a74dde056364aa3bb67fe5efb9f2c72 |
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| Source note | uspto-grants-2010_04 |
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