HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64304Generated: October 25, 2026
Diisopropylamine → Ethyl 1-benzyl-4-(N,N'-di-tert-butyloxycarbonylhydrazino)piperidin-4-ylcarboxylate
https://huagongshe.com/reaction/64304
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Ethyl 1-benzylpiperidine-4-carboxylate | HCID 90423 | — |
| Reactant | Di-tert-butyl azodicarboxylate | HCID 97268 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 1-benzyl-4-(N,N'-di-tert-butyloxycarbonylhydrazino)piperidin-4-ylcarboxylate | HCID 15663644 | 73.3% |
Reaction Steps
To a solution of diisopropylamine (153 mg, 1.5 mmol) in THF (20 mL) was added n-BuLi (2.5 M, 0.6 mL) at −75° C. under N2. After 5 min, ethyl 1-benzylpiperidine-4-carboxylate (247 mg, 1.0 mmol) was added and the resulting mixture then stirred at −70° C. for 10 min, before adding di-tert-butyl azodicarboxylate (345 mg, 1.5 mmol). The reaction was stirred for 30 min, then quenched with aqueous NH4Cl (10 mL) and extracted with EA (10 mL×3). The combined organic layers were dried over Na2SO4 and concentrated to give the crude product (350 mg, 72%) as an off-white solid. MS (ESI, m/e) [M+1]+ 478.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09447106B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-40e74cb1647745cdaf80f338d0e5b93b |
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| Source note | uspto-grants-2016_09 |
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