HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56412Generated: October 26, 2026
Triethylamine → HCID 58745550, compound
https://huagongshe.com/reaction/56412
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzyl succinimido carbonate | HCID 83172 | — |
| Reactant | rac-tert-butyl (3R,4R)-4-amino-3-hydroxypiperidine-1-carboxylate | HCID 10727458 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58745550 | HCID 58745550 | 100% |
Reaction Steps
To a stirred mixture of trans-tert-butyl 4-amino-3-hydroxypiperidine-1-carboxylate (1.05 g, 4.86 mmol) in 80 mL of dichloromethane was added triethyl amine (5.89 g, 5.83 mmol), followed by the addition of N-(benzyloxycarbonyloxy)succinimide (1.27 g, 5.10 mmol) at 0° C. The reaction was stirred at room temperature for 16 hours and then diluted with 100 mL of dichloromethane. The solution mixture was washed with 5% citric acid solution (2×100 mL), 5% potassium carbonate solution (2×100 mL) and brine (200 mL). The organic layer was dried over anhydrous sodium sulfate and filtered, followed by concentration under reduced pressure. The resultant oily matter was purified by silica gel column chromatography (ethyl acetate: petroleum ether=1:4˜1:2) to afford the title compound (1.7 g, ˜100%, crude) as a colorless oil. MS (ES+) C18H26N2O5 requires: 350, found: 251 [M+H−100]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434700B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-fc8d2f407bfa44ec9e002080f9eab6a6 |
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| Source note | uspto-grants-2016_09 |
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