HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341802Generated: October 26, 2026
(Pyrrolidin-3-yl)methanol → benzyl N-[3-(hydroxymethyl)pyrrolidine-1-carboximidoyl]carbamate
https://huagongshe.com/reaction/341802
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | (Pyrrolidin-3-yl)methanol | HCID 13400657 | — |
| Reactant | benzyl N-(C-methoxycarbonimidoyl)carbamate | HCID 139267837 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | benzyl N-[3-(hydroxymethyl)pyrrolidine-1-carboximidoyl]carbamate | HCID 140379085 | 25.2% |
Reaction Steps
1.01 g (0.01 mole) (3RS)-3-hydroxymethyl pyrrolidine and 2.29 g (0.011 mole) N-benzyloxycarbonyl-O-methylisourea was dissolved (the amine not very soluble) in toluene and heated to 60° C. for three hours followed by stirring at room temperature over night. The mixture was evaporated and the 1H-NMR showed that the reaction was not completed. The mixture was therefore dissolved in 15 ml acetonitrile and heated to 60° C. for three hours followed by stirring at room temperature over night. The solvent was evaporated and the mixture was dissolved in CH2Cl2, washed once with water, dried (Na2SO4), filtered and evaporated. The crude product was purified by flash chromatography using CH2Cl2 /MeOH 95/5 as eluent to yield 0.70 g (25%) of the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05856307 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-5b550e99bd8a4e83aecd2baa957c8fb1 |
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| Source note | uspto-grants-1999_01 |
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