HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642957Generated: October 30, 2026
Tetrahydrofuran → HCID 59259718, compound
https://huagongshe.com/reaction/642957
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-Morpholino-1-propanol | HCID 199576 | — |
| Reactant | Tributyl(iodomethyl)stannane | HCID 10862926 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59259718 | HCID 59259718 | 150% |
Reaction Steps
To a mixture of sodium hydride (60%, 278 mg, 6.96 mmol) and tetrahydrofuran (20 ml) was added N-(3-hydroxypropyl)morpholine (963 μl, 6.96 mmol) at room temperature. Then, the reaction mixture was stirred at 45° C. (external temperature) for 10 minutes. To the reaction mixture was added tributyl-iodomethyl-tin (2.0 g, 4.64 mmol) at 0° C. (external temperature). Then, the mixture was stirred at 45° C. for 1 hour. The reaction mixture was cooled at room temperature, diluted with ethyl acetate, washed sequentially with water and an aqueous saturated sodium chloride solution, and dried with anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (NH silica gel, heptane:ethyl acetate=9:1) to obtain the title compound (2.08 g, 6.96 mmol, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696347B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-fdd253d4e90c49f38c3674193535ab65 |
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| Source note | uspto-grants-2010_04 |
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