HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973724Generated: October 30, 2026
Putrescine → Benzyl N-(4-aminobutyl)carbamate
https://huagongshe.com/reaction/973724
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Putrescine | HCID 1045 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Benzyl N-(4-aminobutyl)carbamate | HCID 2783677 | 37.6% |
Reaction Steps
A solution of 46 g of methane sulfonic acid in 50 ml of water was added without exceeding 30° C. to a mixture of 23 g of 1,4-diamino butane and 50 ml of water and the reaction medium was diluted with 140 ml of ethanol. A solution of 39 g of benzyl chloroformate in 50 ml of 1,2-dimethoxy ethane and 100 ml of a 50% aqueous solution of potassium acetate were added alternately at pH 3.5 to 5.0. The additions were made alternately to maintain the pH value between 3.5 and 5.0. The mixture was stirred for 90 minutes at 20° to 25° C. and evaporated under reduced pressure. The residue was poured over 500 ml of water and the insoluble part was filtered off. The filtrate was washed 3 times with 150 ml of benzene, and then 100 ml of 30% sodium hydroxide saturated with sodium chloride were added. After extraction with benzene, the extracts were evaporated to dryness under reduced pressure to obtain 19.10 g of the expected product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05064861 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-21d71e76cd624a2f9595ed4e81f05101 |
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| Source note | uspto-grants-1991_11 |
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