HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833477Generated: October 30, 2026
Sulfuric Acid → 5-(4-Fluorophenoxy)-1-penten-4-ol
https://huagongshe.com/reaction/1833477
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 2-(4-Fluorophenoxy)acetaldehyde | HCID 11051869 | — |
| Catalyst | Allyl bromide | HCID 7841 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 5-(4-Fluorophenoxy)-1-penten-4-ol | HCID 21317573 | 77.2% |
Reaction Steps
To a mixture of ether (50 ml.) and magnesium turnings (4.49 g., 0.185 mole) is added a small amount of allyl bromide (ca. 0.5 g.). The mixture is stirred until Grignard reagent is formed (reflux of ether is a good sign). A solution of allyl bromide (24.2 g., 0.20 mole) and 4-fluorophenoxyacetaldehyde (19.0 g., 0.123 mole) in ether (110 ml.) is then added at such a rate as to maintain the reflux of ether. The resulting mixture is heated at reflux for another hour, cooled in an ice bath, and treated with dilute sulfuric acid (1.6 M, 70 ml.). The organic phase is separated and the aqueous phase is extracted with ether three times. The combined extracts are washed with 5% sodium bicarbonate, dried over anhydrous magnesium sulfate and finally concentrated on a rotary evaporator. The oil residue is vacuum distilled at 73° C./0.03 mm. to afford the desired product (18.6 g., 0.095 mole, 77%). ir (neat) 2.90, 3.22, 3.40, 6.05, 6.20, 6.62, 8.00, 8.25, 10.87, 12.10, 13.14μ; pmr (CCl4)δ2.32 (2H, t, J=6Hz), 2.54 (1H, m), 3.6-4.1 (3H, m), 4.8-5.05(1H, m), 5.05-5.25 (1H, m), 5.4-6.3 (1H, m), 6.6-7.1 (4H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04066675 |
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| Source dataset | uspto-grants-1978_01 |
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| ORD ID | ord-92367ea8702a4ce1a7ddf34677da3bc5 |
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| Source note | uspto-grants-1978_01 |
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