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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494004Generated: November 2, 2026

2-Chloroethanol → HCID 88465312, compound

https://huagongshe.com/reaction/1494004

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroethanolHCID 34—
Reactant3-HydroxypyridineHCID 7971—
ReactantPotassium CarbonateHCID 11430—
ReactantPhenylsulfamateHCID 11030308—
Reactant2-(Pyridin-3-yloxy)ethan-1-olHCID 21908997—
Solvent1,4-DioxaneHCID 31275—
SolventIsopropyl alcohol isopropyl etherHCID 21202047—
ProductHCID 88465312HCID 88465312—

Reaction Steps

A mixture of 4.9 g (0.035 mole) of 2-(3-pyridinyloxy)ethanol[prepared as an oil by procedure of Preparation 21 from 14 g (0.15 mole) of 3-hydroxypyridine, 27 ml (0.40 mole) of 2-chloroethanol and 85 g of potassium carbonate] and 8 g (0.046 mole) of sulfamic acid phenyl ester in 100 ml of dioxane was heated at reflux temperatue for 20 min and the solvent then evaporated. The residue was triturated with 250 ml of acetone, filtered, and the filtrate acidified with a solution of anhydrous hydrogen chloride in isopropyl alcohol and the sticky, brown precipitate collected. The brown solid was redissolved in 125 ml of methanol and diluted with 125 ml of ethanol. The solution was stirred with charcoal, filtered, and the filtrate partially evaporated to give a suspension. The suspension was diluted with isopropyl alcohol-isopropyl ether and filtered. The solid was dried at 50° C. for 18 hr and then at 70° C. for 18 hr in a vacuum oven. The yield was 4.5 g of solid, mp 156°-157° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05025031
Source datasetuspto-grants-1991_06
ORD IDord-4c8fc09c1b5e45bfa7bd54b3d972bc3a
Source noteuspto-grants-1991_06