HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033473Generated: November 3, 2026
Diisoamyl ketone → 1-[7-[4-Methyl-1-(3-methylbutyl)pentylamino]heptyl]piperidine
https://huagongshe.com/reaction/1033473
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisoamyl ketone | HCID 62421 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-Piperidineheptanamine | HCID 11745634 | — |
| Reactant | Ethanol hydrochloride | HCID 21887872 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-[7-[4-Methyl-1-(3-methylbutyl)pentylamino]heptyl]piperidine | HCID 15030044 | — |
Reaction Steps
To a solution of 1.70 g of 2,8-dimethylnonan-5-one and 1.98 g of 1-(7-aminoheptyl)piperidine in 50 ml of methanol was added 6 N hydrochloric acid-ethanol to have a pH value of approx. 7 (pH test paper). To the resulting solution was added under cooling 1.26 g of sodium borohydride all at once. The resulting mixture was stirred under chilling with ice for one hour, and then stirred overnight at room temperature. The reaction mixture was concentrated, and the residue was extracted with chloroform after addition of water and an aqueous sodium hydroxide solution. The chloroform portion was dried and evaporated under reduced pressure to remove the solvent, yielding an oily product. The oily product was purified by silica gel column chromatography (eluent: chloroform-methanol 80:1 to 40:1) to give the desired compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05310902 |
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| Source dataset | uspto-grants-1994_05 |
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| ORD ID | ord-14d5b1583a364bb2ad3dca6faf791f97 |
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| Source note | uspto-grants-1994_05 |
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