HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252984Generated: October 25, 2026
Ethylene Oxide → 3-(4-Chloro-6-morpholin-4-yl-pyrid-2-yl)-propan-1-ol
https://huagongshe.com/reaction/252984
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylene Oxide | HCID 6354 | — |
| Reactant | 2-Methyl-4-chloro-6-morpholino-pyridine | HCID 57550522 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Chloro-6-morpholin-4-yl-pyrid-2-yl)-propan-1-ol | HCID 66841223 | — |
Reaction Steps
2-Methyl-4-chloro-6-morpholino-pyridine (50 mmol) is dissolved in tetrahydrofuran (200 mL). The reaction is chilled to −78° C. under an inert atmosphere. A solution of n-butyllithium in hexanes (24 mL, 2.5M, 60 mmol) is added, and the reaction mixture is stirred for thirty minutes. A solution of oxirane dissolved in tetrahydrofuran (40 mL, 41.5M, 60 mmol) is added, and the reaction is allowed to warm to room temperature while stirring overnight. The solvent is removed under reduced pressure, and the crude material is dissolved in methylene chloride (200 mL) and washed with saturated ammonium chloride (2×50 mL), dried with sodium sulfate, and evaporated to dryness. The compound is purified by column chromatography to give 3-(4-chloro-6-morpholin-4-yl-pyrid-2-yl)-propan-1-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07872005B2 |
|---|
| Source dataset | uspto-grants-2011_01 |
|---|
| ORD ID | ord-e7a53f6e86d348988e18c0437946a856 |
|---|
| Source note | uspto-grants-2011_01 |
|---|