HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991652Generated: October 31, 2026
2-Chloroethanol → 2-(Pyridin-3-yloxy)ethan-1-ol
https://huagongshe.com/reaction/991652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloroethanol | HCID 34 | — |
| Reactant | 3-Hydroxypyridine | HCID 7971 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(Pyridin-3-yloxy)ethan-1-ol | HCID 21908997 | 19% |
Reaction Steps
A mixture of 3-hydroxypyridine (2.00 g, 21 mmol), 2-chloroethanol (1.69 g, 21 mmol) and K2CO3 (8.7 g, 63 mmol) in DMF (10 mL) was stirred at 130° C. for 3 h. After cooling, the black mixture was filtered through a short bed of alumina using acetone as eluent to afford a brown oil which was partitioned between water (30 mL) and CH2Cl2 (40 mL). The aqueous phase was extracted with CH2Cl2 (3×40 mL), and the combined organic extracts were dried over MgSO4 and filtered. The filtrate was concentrated to give 0.55 g (19%) of the title compound as a light brown oil. Anal. (C7H9NO2.0.2 H2O) C, H, N.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06465467B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-15c6255e56044daf9adf8785fdc5501f |
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| Source note | uspto-grants-2002_10 |
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