HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423627Generated: October 30, 2026
4-Piperidinemethanol → {1-[3-(1-Methylethyl)-1,2,4-oxadiazol-5-yl]-4-piperidinyl}methanol
https://huagongshe.com/reaction/423627
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Piperidinemethanol | HCID 420771 | — |
| Reactant | 3-(Propan-2-yl)-5-(trichloromethyl)-1,2,4-oxadiazole | HCID 50986551 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | {1-[3-(1-Methylethyl)-1,2,4-oxadiazol-5-yl]-4-piperidinyl}methanol | HCID 57930076 | 34.1% |
Reaction Steps
A solution of 3-(1-methylethyl)-5-(trichloromethyl)-1,2,4-oxadiazole (prepared as in Example 158, Alternative synthesis, Step 3, 179 g, 0.78 mol) in MeOH (300 mL) was treated with 4-piperidinemethanol (108 g, 0.94 mol) and stirred and heated at 50° C. overnight. The solvent was removed and the residue was purified by flash chromatography on a silica gel column to give {1-[3-(1-methylethyl)-1,2,4-oxadiazol-5-yl]-4-piperidinyl}methanol (60 g, 34%) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101634B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-64109180c6cf4a6ebad82578caba18e2 |
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| Source note | uspto-grants-2012_01 |
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