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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073635Generated: October 31, 2026

4-Hydroxybenzyl Alcohol → HCID 14573506, compound

https://huagongshe.com/reaction/2073635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzyl AlcoholHCID 125—
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 14533171HCID 14533171—
SolventEthanolHCID 702—
ProductHCID 14573506HCID 1457350696.8%

Reaction Steps

In a round-bottomed flask, a solution of 2.4 g of p-hydroxybenzyl alcohol in 10 ml of ethanol and 5.3 g of (+)-3-trifluoromethylheptyl p-toluenesulfonate were placed, and a solution of 0.8 g of sodium hydroxide in 10 ml of ethanol was added thereto dropwise, followed by 6 hours of heat-refluxing, cooling by standing and acidification with hydrochloric acid. The organic layer was extracted with diethyl ether. The resultant ether solution was dried with sodium sulfate and subjected to distilling-off of the solvent and purification by silica gel column chromatography to obtain 4.4 g of (+)-p-(3-trifluoromethylheptyloxy)benzyl alcohol. [α]D28 +1.0°, [α]43527 +2.4° (c 5.0, chloroform).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04918213
Source datasetuspto-grants-1990_04
ORD IDord-5689b4a107b640fb8ada2051e099267c
Source noteuspto-grants-1990_04