HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429819Generated: October 30, 2026
Water → (1-(Methylsulfonyl)piperidin-4-yl)methanol
https://huagongshe.com/reaction/429819
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl 1-(methylsulfonyl)piperidine-4-carboxylate | HCID 669104 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1-(Methylsulfonyl)piperidin-4-yl)methanol | HCID 18352755 | 82.1% |
Reaction Steps
A solution of 1.0 M lithium aluminum hydride (200 ml, 0.2 mole) in tetrahydrofuran was added dropwise to a solution of 1-methanesulfonylpiperidine-4-carboxylic acid ethyl ester (68 grams, 0.29 mole) in tetrahydrofuran (500 ml) at about +5° C. The reaction mixture was stirred at 5-10° C. for 15 minutes. Water (10 ml) was added dropwise and the mixture was filtered. The filtrate was concentrated under reduced pressure and triturated with 50% ethyl ether-hexane (100 ml). The resulting white solid was collected and dried to give 1-methanesulfonylpiperidine-4-methanol (46 grams, 82%), m.p. 96-97° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06319920B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-cc3d3a4026a64e65a09748f3365d0819 |
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| Source note | uspto-grants-2001_11 |
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