(1R)-1-(4-Chlorophenyl)propan-1-amine hydrochloride

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(1R)-1-(4-Chlorophenyl)propan-1-amine hydrochloride Basic information
Product Name:(1R)-1-(4-Chlorophenyl)propan-1-amine hydrochloride
Synonyms:(R)-1-(4-Chlorophenyl)-1-propanamine Hydrochloride;(R)-1-(4-chlorophenyl)propyl-1-aminehydrochloride;(1R)-1-(4-Chlorophenyl)propan-1-amine hydrochloride
CAS:1448902-18-8
MF:C9H13Cl2N
MW:206.11222
EINECS:
Product Categories:
Mol File:1448902-18-8.mol
(1R)-1-(4-Chlorophenyl)propan-1-amine hydrochloride Structure
(1R)-1-(4-Chlorophenyl)propan-1-amine hydrochloride Chemical Properties
storage temp. Sealed in dry,Room Temperature
Safety Information
MSDS Information
(1R)-1-(4-Chlorophenyl)propan-1-amine hydrochloride Usage And Synthesis
Synthesis
2-Propanesulfinamide, N-[(1R)-1-(4-chlorophenyl)propyl]-2-methyl-, [S(S)]-

1448902-54-2

(1R)-1-(4-CHLOROPHENYL)PROPAN-1-AMINE HYDROCHLORIDE

1448902-18-8

General procedure for the synthesis of (R)-1-(4-chlorophenyl)propan-1-amine hydrochloride using compound (CAS: 1448902-54-2) as starting material: to a methanol solution (3.60 mL) of 40a (1.93 g, 7.22 mmol) was added slowly at room temperature a solution of 1,4-dioxane in 4 N HCl (3.60 mL, 14.4 mmol). The reaction mixture was stirred at room temperature for 40 minutes. After completion of the reaction, ether (Et2O) was added to the mixture and the resulting precipitate was collected by filtration to afford the target product 29a (1.30 g, 90% yield) as a colorless solid. The product was characterized by 1H NMR (500 MHz, CD3OD): δ 7.49-7.41 (m, 5H), 4.31 (dd, J = 10.0, 5.6 Hz, 1H), 1.93 (ddd, J = 15.6, 10.3, 5.4 Hz, 1H), 1.81-1.75 (m, 1H), 1.44-1.36 (m, 1H), and 0.96 (d, J = 6.8 Hz, 3H), 0.92 (d, J = 6.8 Hz, 3H).

References[1] Bioorganic and Medicinal Chemistry, 2013, vol. 21, # 18, p. 5907 - 5922
(1R)-1-(4-Chlorophenyl)propan-1-amine hydrochloride Preparation Products And Raw materials
Raw materials2-Propanesulfinamide, N-[(1R)-1-(4-chlorophenyl)propyl]-2-methyl-, [S(S)]--->Methanol-->Hydrochloric acid-->1,4-Dioxane
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