HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714124Generated: October 26, 2026
Potassium Carbonate → Tert-butyl 4-(cyclopropylmethyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/714124
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (Chloromethyl)cyclopropane | HCID 80013 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 4-(cyclopropylmethyl)piperazine-1-carboxylate | HCID 46743082 | — |
Reaction Steps
1-Tertbutoxycarbonylpiperazine (6a) (1.86 g, 10 mmol) was dissolved in dichloromethane (20 mL), and anhydrous potassium carbonate (829 mg, 6 mmol) was added. The dichloromethane solution of chloromethyl cyclopropane (7a) (1.1 mL, 12 mmol) was added dropwise, and reacted overnight at room temperature, after that, the reaction mixture was washed with water. The water layer was extracted with dichloromethane for twice, the organic phases were combined, washed successively with 50 mL saturated sodium bicarbonate solution and saturated sodium chloride solution for three times, dried with anhydrous sodium sulfate. Column chromatography (petroleum ether:ethyl acetate 2:1) was performed to isolate white solid powder 1-tertbutoxycarbonyl-4-(cyclopropylmethyl)piperazine (7b), 2.01 g white solid (yield 79.0%). ESI-MS m/z calculated for: 240.18. found: 241.05 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187430B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-a7d66c35fb7446b5992eb239529631d2 |
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| Source note | uspto-grants-2015_11 |
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