HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458651Generated: October 30, 2026
Acetic Acid → 1-benzyl-N,4-dimethylpiperidin-3-amine
https://huagongshe.com/reaction/458651
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-benzyl-N,4-dimethylpiperidin-3-amine | HCID 9943889 | 87.75% |
Reaction Steps
To a stirred solution of the product from Method E (3.81 grams/0.019 mol) and 38 mL of 2.0 M methylamine in THF was added 2.2 mL of acetic acid and the resulting mixture stirred at room temperature for 1.5 hours. Triacetoxysodiumborohydride (NaB(OAc)3H) (7.94 grams/0.038 mol) was added as a solid and the new mixture stirred at room temperature for 18 hours. The reaction was quenched with 2 N hydrochloric acid and the pH adjusted to 1. The reaction mixture was washed two times with ether, the aqueous layer then adjusted to pH of 12 with 6 N sodium hydroxide (aq) and extracted three times with dichloromethane The combined dichloromethane layers were dried over Na2SO4, filtered and evaporated to dryness in vacuo affording 3.51 grams (87.75%) of the title compound as dark yellow oil. LRMS: 219.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07192963B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-99da70a9dcf64445b519911709629c89 |
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| Source note | uspto-grants-2007_03 |
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