HuagongsheHuagongshe Chemistry Print Report · For research reference only
Putrescine → Benzyl N-(4-aminobutyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Putrescine | HCID 1045 | — |
| Reactant | Benzyl S-4,6-dimethylpyrimidin-2-yl thiocarbonate | HCID 563496 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Benzyl N-(4-aminobutyl)carbamate | HCID 2783677 | 23% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04518802 |
| Source dataset | uspto-grants-1985_05 |
| ORD ID | ord-3ada78469249495ea31384774e4b3f03 |
| Source note | uspto-grants-1985_05 |