HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179750Generated: October 30, 2026
Potassium Carbonate → HCID 86650116, compound
https://huagongshe.com/reaction/2179750
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Benzylpiperidine | HCID 31738 | — |
| Reactant | HCID 86650113 | HCID 86650113 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86650116 | HCID 86650116 | 124.5% |
Reaction Steps
To a stirred solution of ((1R,4S)-4-(tert-butoxycarbonylamino)cyclopent-2-enyl)methyl 4-methylbenzenesulfonate (step 1, about 0.5 g) in DCM (50 ml), potassium carbonate (about 0.3 g) was added at room temperature and cooled to about 0° C. After ten minutes, 4-benzylpiperidine (0.17 g) was added and stirred the reaction at room temperature for about 6 hours. Completion of the reaction was monitored by TLC. The reaction mixture was neutralized and extracted with DCM, the organic layer was dried over Na2SO4 and concentrated under reduced pressure to furnish the title compound (0.45 g) as light yellow liquid. 1H NMR (300 MHz, CDCl3: 1.24-1.29 (m, 1H); 1.39-1.40 (s, 9H); 2.29-2.60 (m, 7H); 2.79-2.80 (m, 1H); 3.70-3.73 (m, 4H); 4.63 (S, 1H); 5.37-5.39 (d, J=6 Hz, 1H); 5.72-5.81 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09067966B2 |
|---|
| Source dataset | uspto-grants-2015_06 |
|---|
| ORD ID | ord-4c5ac804ec6b42068e8e5d1bfa3beb77 |
|---|
| Source note | uspto-grants-2015_06 |
|---|