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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 612814Generated: October 31, 2026

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

https://huagongshe.com/reaction/612814

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxybenzyl AlcoholHCID 125—
ReactantTolueneHCID 1140—
ReactantPiperidine, 1-(2-chloroethyl)-, hydrochlorideHCID 74826—
CatalystBenzyltriethylammonium bromideHCID 165294—
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 (SN, 30 mL). Toluene (30 mL) was added followed by 1-(2-chloroethyl) piperidine hydrochloride (9.29 g, 0.05 mol) and benzyltriethylammonium 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 numberUS06005102
Source datasetuspto-grants-1999_12
ORD IDord-65b1e7d3fc794e8282339830fb07881d
Source noteuspto-grants-1999_12