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ChemicalBook CAS DataBase List 1-Amino-1-(hydroxymethyl)cyclopropane hydrochloride
115652-52-3

1-Amino-1-(hydroxymethyl)cyclopropane hydrochloride synthesis

1synthesis methods
tert-Butyl (1-(hydroxymethyl)cyclopropyl)carbamate

107017-73-2

1-Amino-1-(hydroxymethyl)cyclopropane hydrochloride

115652-52-3

8.2 Synthesis of 1-aminocyclopropane methanol hydrochloride 1.04 g of tert-butyl (1-hydroxymethylcyclopropyl)-carbamate was dissolved in 5 mL of dioxane. Under stirring, 2.5 mL of 4 mol/L HCl in dioxane solution was added slowly and dropwise. The reaction mixture was stirred at room temperature for 15 hours. Subsequently, the solvent was evaporated to half of the original volume and the precipitated solid was collected by filtration. 0.5 g of the target product 1-aminocyclopropanemethanol hydrochloride was finally obtained. The structure of the product was confirmed by 1H NMR (400 MHz, DMSO): δ 5.27 (1H, t), 0.91 (2H, t), 0.71 (2H, t).

107017-73-2 Synthesis
tert-Butyl (1-(hydroxymethyl)cyclopropyl)carbamate

107017-73-2
205 suppliers
$8.00/100mg

-

Yield:-

Reaction Conditions:

with hydrogenchloride in 1,4-dioxane at 20;

Steps:

8.2 8.2 1-aminocyclopropanemethanol
8.2 1-aminocyclopropanemethanol 1.04 g tert-butyl (1-hydroxymethylcyclopropyl)-carbamidate are placed in 5 ml dioxane. 2.5 ml HCl in dioxane (4 mol/l) are added dropwise. The reaction mixture is stirred for 15 h at ambient temperature. The solvent is evaporated down by half and the precipitated solid is suction filtered. 0.5 g product are obtained as the hydrochloride. 1H NMR (400 MHz, DMSO): 5.27 (1H, t); 0.91 (2H, t); 0.71 (2H, t).

References:

BOEHRINGER INGELHEIM INTERNATIONAL GMBH US2010/305102, 2010, A1 Location in patent:Page/Page column 16

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