HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238444Generated: October 26, 2026
Acetic Acid → 1-Methyl-4-(3-nitro-6-pentafluoroethyl-phenoxymethyl)-piperidine
https://huagongshe.com/reaction/238444
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 4-(3-Nitro-6-pentafluoroethyl-phenoxymethyl)-piperidine | HCID 21959389 | — |
| Reactant | Formaldehyde--water (1/1) | HCID 22136924 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Methyl-4-(3-nitro-6-pentafluoroethyl-phenoxymethyl)-piperidine | HCID 22249451 | — |
Reaction Steps
4-(3-Nitro-6-pentafluoroethyl-phenoxymethyl)-piperidine (316.5 mg) was dissolved in 2.7 mL acetonitrile, then added 37% formaldehyde/H2O (360 ul) and then NaBH3CN (90 mg). Upon addition of NaCNBH3 the reaction exothermed slightly. The reaction was stirred at RT and pH was maintained at ˜7 by addition of drops of glacial acetic acid. After about 1 h, the mixture was concentrated in vacuo, treated with 8 mL 2N KOH and extracted two times with 10 mL Et2O. The organic layers were washed with 0.5N KOH and then the combined organic layers were extracted two times with 1N HCl. The aqueous layer was basified with solid KOH and extracted two times with Et2O. This organic layer was then washed with brine/1N NaOH, dried over Na2SO4, filtered, concentrated in vacuo and dried under high vacuum to give pure compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642624B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-7a98c2e7fc7f4dc686b47143090b3399 |
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| Source note | uspto-grants-2014_02 |
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