HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822170Generated: October 31, 2026
Ethyl Bromide → 1-(3-Fluorophenyl)propan-1-ol
https://huagongshe.com/reaction/1822170
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | 3-Fluorobenzaldehyde | HCID 68009 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(3-Fluorophenyl)propan-1-ol | HCID 20642621 | — |
Reaction Steps
18 L ethyl bromide were dissolved in 30 L of THF and added dropwise to a suspension of 6 kg of magnesium in 30 L of THF. The reaction solution was next stirred for two hours at 65° to 75° C. and then cooled to 0 to 10° C. 15 kg of 3-fluorobenzaldehyde in 60 L of THF were added while cooling with ice over a period of 6 hr and the reaction solution was stirred overnight at room temp. The reaction solution was quenched with saturated ammonium chloride solution at 0°-10° C. The reaction solution was stirred for one hour, organic layer separated and concentrated. The concentrate was extracted with 40 L of DCM and washed with 30 L of 5% HCl solution. The solvent was removed in vacuo. After drying, 20 kg of 1-(3-Fluoro -phenyl)-propan-1-ol were obtained as a brown oil and taken as such to the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07608740B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-34780d2d851d46e1807c9ffdb822e700 |
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| Source note | uspto-grants-2009_10 |
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