HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456450Generated: October 30, 2026
Acetyl chloride → 1-(3-Hydroxypiperidin-1-yl)ethan-1-one
https://huagongshe.com/reaction/456450
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Hydroxypiperidine | HCID 23293 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(3-Hydroxypiperidin-1-yl)ethan-1-one | HCID 21897030 | 83.1% |
Reaction Steps
3-Hydroxypiperidine (3.0 g, 30.0 mmol) was dissolved in THF (40 mL) and methylene chloride (40 mL). Triethylamine (7.47 g, 74.0 mmol) was added. The mixture was cooled to −78° C. and acetyl chloride (2.35 g, 30.0 mmol) was added drop wise. The mixture was warmed to r.t. and stirred under nitrogen for 1 about an hour. The solvents were removed under reduced pressure, and the resulting oil was purified using silica chromatography (2% methanol in ethyl acetate) to afford the title compound (3.57 g, 83%) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07186715B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-ee7f708a522c4e49b678cf3f9f315113 |
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| Source note | uspto-grants-2007_03 |
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