1-Amino-1-(hydroxymethyl)cyclopropane hydrochloride
1-Amino-1-(hydroxymethyl)cyclopropane hydrochloride Basic information
- Product Name:
- 1-Amino-1-(hydroxymethyl)cyclopropane hydrochloride
- Synonyms:
-
- 1-Amino-1-(hydroxymethyl)cyclopropane hydrochloride
- 1-Aminocyclopropanemethanol hydrochloride
- (1-Aminocyclopropyl)methanol hydrochloride, 98%
- CyclopropaneMethanol, 1-aMino- (hydrochloride)(1:1)
- (1-AMINOCYCLOPROPYL)METHANOL HCL
- [1-(hydroxymethyl)cyclopropyl]azanium chloride
- 1-Amino-cyclopropanemethanol·HCL
- [1-(hydroxymethyl)cyclopropyl]azanium
- CAS:
- 115652-52-3
- MF:
- C4H9NO.HCl
- MW:
- 123.58
- EINECS:
- 808-869-5
- Mol File:
- 115652-52-3.mol
1-Amino-1-(hydroxymethyl)cyclopropane hydrochloride Chemical Properties
- Melting point:
- 119 ºC (DEC.)
- storage temp.
- Inert atmosphere,Room Temperature
- Appearance
- White to off-white Solid
- InChI
- InChI=1S/C4H9NO.ClH/c5-4(3-6)1-2-4;/h6H,1-3,5H2;1H
- InChIKey
- ULEMJGCUGKDKTD-UHFFFAOYSA-N
- SMILES
- C1(N)(CO)CC1.[H]Cl
1-Amino-1-(hydroxymethyl)cyclopropane hydrochloride Usage And Synthesis
Synthesis
107017-73-2
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).
References
[1] Journal of Medicinal Chemistry, 1988, vol. 31, # 10, p. 2004 - 2008
[2] European Journal of Organic Chemistry, 2005, # 11, p. 2250 - 2258
[3] Patent: US2010/305102, 2010, A1. Location in patent: Page/Page column 16
[4] Patent: US2011/21501, 2011, A1. Location in patent: Page/Page column 59
[5] Patent: US2011/28441, 2011, A1. Location in patent: Page/Page column 14
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