Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloroethanol | HCID 34 | — |
| Reactant | 3-Hydroxypyridine | HCID 7971 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phenylsulfamate | HCID 11030308 | — |
| Reactant | 2-(Pyridin-3-yloxy)ethan-1-ol | HCID 21908997 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Solvent | Isopropyl alcohol isopropyl ether | HCID 21202047 | — |
| Product | HCID 88465312 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05025031 |
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| Source dataset | uspto-grants-1991_06 |
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| ORD ID | ord-4c8fc09c1b5e45bfa7bd54b3d972bc3a |
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| Source note | uspto-grants-1991_06 |
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