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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(4-aminobutyl)carbamateHCID 4351—
ReactantN-CarbethoxyphthalimideHCID 31187—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 15314931HCID 1531493159%

Reaction Conditions

Temperature52.5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069149
Source datasetuspto-grants-2000_05
ORD IDord-452f47a9fdd547bcb7aa21e1159c01e5
Source noteuspto-grants-2000_05