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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463449Generated: October 29, 2026

Putrescine → Benzyl N-(4-aminobutyl)carbamate

https://huagongshe.com/reaction/463449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPutrescineHCID 1045—
ReactantBenzyl S-4,6-dimethylpyrimidin-2-yl thiocarbonateHCID 563496—
SolventMethanolHCID 887—
ProductBenzyl N-(4-aminobutyl)carbamateHCID 278367723%

Reaction Steps

Into 30 mL of 50% aqueous methanol, was dissolved 1.76 g (20 mmoles) of 1,4-butanediamine followed by the addition of 5.48 g (20 mmoles) of S-benzyloxycarbonyl-4,6-dimethyl-2-mercaptopyrimidine (a product of Kokusan Kagaku Co.). The mixture was stirred for 3 hours. Thereafter, the reaction mixture was filtered to remove the precipitated di-N-benzyloxycarbonyl compound [2.09 g (29%) were recovered], and the filtrate was evaporated to dryness. The residue was dissolved in 250 mL of chloroform, washed 5 times with 100 mL of water. The chloroform layer was dried over anhydrous sodium sulfate, and evaporated to dryness to obtain 1.0 g (23% yield) of mono-N-benzyloxycarbonyl-1,4-butanediamine in colorless syrup form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04518802
Source datasetuspto-grants-1985_05
ORD IDord-3ada78469249495ea31384774e4b3f03
Source noteuspto-grants-1985_05