HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108651Generated: November 1, 2026
tert-butyl N-(4-aminobutyl)carbamate → HCID 15314931, compound
https://huagongshe.com/reaction/1108651
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-butyl N-(4-aminobutyl)carbamate | HCID 4351 | — |
| Reactant | N-Carbethoxyphthalimide | HCID 31187 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 15314931 | HCID 15314931 | 59% |
Reaction Steps
5.41 g (28.74 mmol) of N-(tert-butoxycarbonyl)-1,4-diaminobutane was dissolved in 100 ml of 1,4-dioxane and 4.86 g (28.74 mmol) of N-carboethoxyphthalimide was added thereto. The mixture was heated at 45 to 60° C. and stirred for 4 hours. After the reaction mixture was concentrated under reduced pressure, 1N hydrochloric acid was added thereto and the resulting solution was extracted with ethyl acetate. The extract was washed with brine and dried (Na2SO4). The solvent was distilled off and the residue was purified by silica gel column chromatography (chloroform:methanol=200:1 (v/v)) to obtain 5.40 g (16.96 mmol) of N-[4-(tert-butoxycarbonylamino)butyl]phthalimide as a white solid. Its spectroscopic data are as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06069149 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-452f47a9fdd547bcb7aa21e1159c01e5 |
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| Source note | uspto-grants-2000_05 |
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