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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 903553Generated: October 30, 2026

2-(Benzyloxy) ethanol → HCID 23336639, compound

https://huagongshe.com/reaction/903553

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Benzyloxy) ethanolHCID 12141—
Reactant2902-98-9HCID 17941—
Reactant1-Methyl-3-pyrrolidinolHCID 93074—
SolventPyridineHCID 1049—
ProductHCID 23336639HCID 2333663953.8%

Reaction Steps

A mixture of chlorodiphenylacetyl chloride (20 g), 1-methyl-3-pyrrolidinol (7.6 g), and pyridine (35 g) is kept at room temperature for two hours. After adding 45 g of 2-benzyloxyethanol, the mixture is refluxed gently for 18 hours. Excess pyridine and benzyloxyethanol are distilled off under reduced pressure, the residue is dissolved in ether and washed twice with water. The organic phase is dried over magnesium sulfate (MgSO4), filtered and the filtrate evaporated to dryness. Chromatography of the residue on the silica gel with ethyl acetate-hexane-triethylamine (50:50:1) as eluent affords 18 g of 1-methyl-3-[2,2-diphenyl-2-(2-benzyloxyethoxy)acetoxy]pyrrolidine as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04228171
Source datasetuspto-grants-1980_10
ORD IDord-76dd6a197ada47d181bfacd248bb8645
Source noteuspto-grants-1980_10