HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482280Generated: October 29, 2026
Sodium Hydroxide → HCID 53988844, compound
https://huagongshe.com/reaction/482280
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 11837562 | HCID 11837562 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53988844 | HCID 53988844 | 97.8% |
Reaction Steps
A stirred solution of 10.0 grams (0.018 mole) of N-[4-(cyclopropylmethoxy)phenylmethyl]-4-[bis(4-trifluoromethylphenyl)hydroxymethyl]piperidine in methylene chloride was cooled to 0° C., and 3.1 grams (0.01 2 mole) of 50% 3-chloroperoxybenzoic acid was added in two portions. Upon completion of the addition the reaction mixture was allowed to warm to ambient temperature, where it stirred for about 18 hours. After this time, the reaction mixture was poured into aqueous 5% sodium hydroxide solution. The organic layer was separated and washed with aqueous 5% sodium hydroxide solution. The organic layer was then filtered through phase separated silicone treated paper. The filtrate was concentrated under reduced pressure, yielding 10.2 grams of N-[4-(cyclopropylmethoxy)phenylmethyl]-4-[bis(4-trifluoromethylphenyl)hydroxy-methyl]piperidine N-oxide. The NMR spectrum was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05795901 |
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| Source dataset | uspto-grants-1998_08 |
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| ORD ID | ord-89eac9321f9f4be8bff49b44e4243d5d |
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| Source note | uspto-grants-1998_08 |
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