Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 4-[[(1,1-dimethylethoxy)carbonyl]amino]Butanoic acid methyl ester | HCID 13112352 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 860653-06-1 | HCID 57829537 | 90% |
Reaction Steps
To a solution of methyl 4-(tert-butoxycarbonylamino)butanoate (21.0 g, 96.8 mmol) in MeOH (180 mL) was added NH2NH2.H2O (28.0 g, 483 mmol) at rt. The mixture was stirred at 65° C. for 12 hrs then concentrated under reduced pressure. The crude material was dissolved in DCM (400 mL). The organic layer was washed with water (2×), and saturated sodium chloride (2×), dried over Na2SO4, and concentrated to afford tert-butyl 4-hydrazinyl-4-oxobutylcarbamate (18.9 g, 90%) as a white solid. ESI-MS (EI+, m/z): 240 [M+Na]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962844B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-9dd06960fb514fe392f14d5b4ec53565 |
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| Source note | uspto-grants-2015_02 |
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