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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702602Generated: October 26, 2026

Hydrochloric Acid → alpha-Allenyl-3-phenoxybenzyl alcohol

https://huagongshe.com/reaction/1702602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantDiisopropylamineHCID 7912—
Reactant3-Phenoxy-alpha-ethynylbenzylalcoholHCID 12919092—
Solvent1,4-DioxaneHCID 31275—
Productalpha-Allenyl-3-phenoxybenzyl alcoholHCID 13104645—

Reaction Conditions

Temperature20 °C

Reaction Steps

10 g of α-ethynyl-3-phenoxybenzyl alcohol, 2.1 g of paraformaldehyde, 5.3 g of diisopropylamine, 0.215 g of CuBr and 50 ml of dioxane are refluxed for 2 hours. The reaction mixture is cooled to 20° C., poured into a solution of 2 N HCl and extracted with ether. The organic phase is washed with 10% potassium carbonate and saturated sodium chloride solution, dried over magnesium sulfate and concentrated. The residue is chromatographed over silica gel with a 7:3 mixture of hexane/ether as eluant, affording the compound of the formula ##STR5## with a refractive index of nD20° =1.5942.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04348408
Source datasetuspto-grants-1982_09
ORD IDord-bef36a2472e643a9af1854f541dd8bdf
Source noteuspto-grants-1982_09