HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494014Generated: October 30, 2026
4,4'-Bipiperidine dihydrochloride → 4,4'-Bipiperidine, 1-boc protected
https://huagongshe.com/reaction/494014
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4,4'-Bipiperidine dihydrochloride | HCID 12270637 | — |
| Reactant | Tert-butyldicarbonate | HCID 22064466 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 4,4'-Bipiperidine, 1-boc protected | HCID 11747599 | 72% |
Reaction Steps
A solution is prepared of 41 g (0.17 M) of 4,4′-bipiperidine dihydrochloride in 250 ml of ethanol and 250 ml of 2N sodium hydroxide. A solution of 18.5 g (0.085 M) of t-butyl dicarbonate in 100 ml of ethanol are added slowly, at 0° C. The reaction mixture is agitated for 1 hour at 10° C. and the ethanol is then removed by an evaporator, under reduced pressure. The residual aqueous phase is saturated with sodium chloride and extracted with ethyl acetate. The organic phase obtained is dried over magnesium sulphate and concentrated under reduced pressure. The crude product is purified by silica gel chromatography in eluting with the aid of a dichloromehane/methanol/aqueous ammonia mixture (8/2/0.4; v/v/v). 16.5 g of the compound sought after are thus obtained as a white solid (yield=72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07538111B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-c75086f5b7984dd5a4371536ebd168c0 |
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| Source note | uspto-grants-2009_05 |
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