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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066427Generated: November 3, 2026

4-Hydroxybenzyl Alcohol → [4-(2-Piperidin-1-ylethoxy)phenyl]methanol

https://huagongshe.com/reaction/1066427

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzyl AlcoholHCID 125—
ReactantBromide ionHCID 259—
ReactantTolueneHCID 1140—
ReactantPiperidine, 1-(2-chloroethyl)-, hydrochlorideHCID 74826—
SolventSodium HydroxideHCID 14798—
Product[4-(2-Piperidin-1-ylethoxy)phenyl]methanolHCID 981610775%

Reaction Steps

4-hydroxybenzyl alcohol (6.2 g, 0.0.05 mol) was dissolved in aqueus sodium hydroxide (5N, 30 mL). Toluene (30 mL) was added followed by 1-(2-chloroethyl)piperidine hydrochloride (9.29 g, 0.05 mol) and benzyltriethylamumonium bromide (0.3 g). The reaction mixture was heated with vigorous stirring for 1.5 h. The layers were separated, the aqueous layer was extracted with toluene (2×15 mL). Combined organic extracts and organic layer was washed with water (50 mL), brine (50 mL), dried over sodium sulfate, and concentrated on a rotary evaporator to give 8.725 g (75%) of alcohol (3a) as a yellowish brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06242605B1
Source datasetuspto-grants-2001_06
ORD IDord-f9bff3e7ba3d4bfbba34d11bf22c8167
Source noteuspto-grants-2001_06