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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1967071Generated: October 31, 2026

Hydrochloric Acid → 4-Phenylbut-3-en-2-ol

https://huagongshe.com/reaction/1967071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantBenzenemethanol, alpha-1-propen-1-yl-HCID 219674—
ReactantSodium BicarbonateHCID 516892—
Solvent1,4-DioxaneHCID 31275—
Product4-Phenylbut-3-en-2-olHCID 1517296.8%

Reaction Steps

1-Phenyl-2-buten-1-ol (135.88 g) was dissolved in 2300 mL of dioxane and treated with 2750 mL of dilute hydrochloric acid (2.3 mL of concentrated hydrochloric acid in 2750 mL of water) at room temperature. The mixture was stirred overnight and then poured into 4333 mL of ether and neutralized with 2265 mL of saturated aqueous sodium bicarbonate. The aqueous phase was extracted with 1970 mL of ether. The combined extract was dried over anhydrous potassium carbonate. Evaporation of the solvent followed by Kugelrohr distillation at 30° C. for 30 minutes afforded 131.73 g (96.8%) of the desired 4-phenyl-3-buten-2-ol as an oil which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420698B2
Source datasetuspto-grants-2013_04
ORD IDord-08f1b0909fc7406fb34435bed6118a75
Source noteuspto-grants-2013_04