HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066882Generated: November 1, 2026
HCID 57461146, compound → HCID 141306036, compound
https://huagongshe.com/reaction/2066882
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57461146 | HCID 57461146 | — |
| Reactant | HCID 67512109 | HCID 67512109 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 141306036 | HCID 141306036 | — |
Reaction Steps
3-Boc-piperidinone (0.83 mmol) and NaOAc.3H2O (30 mg) were combined in 1 mL of ethanol and heated to 65° C. for 15 minutes. 2b (167 mg, 0.83 mmol) was added and the mixture was heated at 65° C. for 18 h. The mixture was concentrated, taken up with DCM (5 mL), washed with aqueous NaHCO3 (5 mL) and the organic layer was separated and treated with TFA (5 mL). The mixture was stirred at room temperature for 45 minutes, concentrated, diluted with NaHCO3 (8 mL) and extracted with EtOAc (2×5 mL). The extracts were dried and concentrated to afford the crude 61a: LC-MS 284.2 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08293729B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-c566d155810e489d948df75b7f0f2f59 |
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| Source note | uspto-grants-2012_10 |
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