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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1957143Generated: November 3, 2026

(Pyrrolidin-3-yl)methanol → benzyl N-[3-(hydroxymethyl)pyrrolidine-1-carboximidoyl]carbamate

https://huagongshe.com/reaction/1957143

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Pyrrolidin-3-yl)methanolHCID 13400657—
Reactantbenzyl N-(C-methoxycarbonimidoyl)carbamateHCID 139267837—
SolventTolueneHCID 1140—
Productbenzyl N-[3-(hydroxymethyl)pyrrolidine-1-carboximidoyl]carbamateHCID 14037908525.2%

Reaction Conditions

Temperature60 °C

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 solvebt was evaporated and the mixture was dissolved in CH2Cl2, washed once with water, dried (Na2 SO4), 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05783563
Source datasetuspto-grants-1998_07
ORD IDord-c1c3a5a956494827850ff70bb583be15
Source noteuspto-grants-1998_07