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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantAllyl bromideHCID 7841—
ReactantMagnesiumHCID 5462224—
Reactant2-(4-Fluorophenoxy)acetaldehydeHCID 11051869—
CatalystAllyl bromideHCID 7841—
SolventDiethyl EtherHCID 3283—
Product5-(4-Fluorophenoxy)-1-penten-4-olHCID 2131757377.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04066675
Source datasetuspto-grants-1978_01
ORD IDord-92367ea8702a4ce1a7ddf34677da3bc5
Source noteuspto-grants-1978_01