(R)-3-Aminopyrrolidine CAS 116183-82-5

Introduction:Basic information about (R)-3-Aminopyrrolidine CAS 116183-82-5, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

(R)-3-Aminopyrrolidine Basic information

Product Name:(R)-3-Aminopyrrolidine
Synonyms:(3R)-Pyrrolidine-3-amine;(3R)-pyrrolidin-3-aMine;(R)-(+)-3-Aminopyrrolidine 98%;3-amino-R-pyrrolidine;(3R)-3-Pyrrolidinamine;(3R)-(+)-3-AMINOPYRROLIDINE 98+%;(R)-pyrrolidin-3-amine;(r)-(R)-3-AMinopyrrolidine
CAS:116183-82-5
MF:C4H10N2
MW:86.14
EINECS:
Product Categories:Chiral Building Blocks;Heterocyclic Building Blocks;3-Aminopyrrolidines;Amines (Chiral);Chiral 3-Aminopyrrolidines;Pyrrolidines;pharmacetical;Pyrrole&Pyrrolidine&Pyrroline;API intermediates;Chiral Building Blocks;Synthetic Organic Chemistry;Chiral Compound
Mol File:116183-82-5.mol

(R)-3-Aminopyrrolidine Chemical Properties

Boiling point 164-165 °C(lit.)
density 0.984 g/mL at 25 °C(lit.)
refractive index n20/D 1.489(lit.)
Fp 147 °F
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka9.94±0.20(Predicted)
form clear liquid
color Colorless to Almost colorless
Optical Rotation[α]/D +20°, neat
InChI1S/C4H10N2/c5-4-1-2-6-3-4/h4,6H,1-3,5H2/t4-/m1/s1
InChIKeyNGXSWUFDCSEIOO-SCSAIBSYSA-N
SMILESN[C@@H]1CCNC1
CAS DataBase Reference116183-82-5(CAS DataBase Reference)

Safety Information

Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
RIDADR NA 1993 / PGIII
WGK Germany 3
HazardClass 8
PackingGroup III
HS Code 29339900
Storage Class8A - Combustible corrosive hazardous materials
Hazard ClassificationsEye Dam. 1
Skin Corr. 1B

(R)-3-Aminopyrrolidine Usage And Synthesis

Synthesis

114715-38-7

79286-79-6

General procedure for the synthesis of (S)-3-aminopyrrolidine from (S)-1-benzyl-3-aminopyrrolidine: 7.0 g of (S)-1-benzyl-3-aminopyrrolidine, 25 mL of methanol, and 0.7 g of 5% Pd/C catalyst were added to a 100 mL autoclave. The hydrogen pressure was adjusted to 1 MPa, the temperature was raised to 70 °C and the reaction was kept stirring for 8 hours. Upon completion of the reaction, it was cooled to room temperature and the pressure was slowly released. The reaction mixture was filtered to remove the catalyst and the mother liquor was concentrated and purified by distillation to collect the 80-83 °C/40 kPa fraction to give 3.2 g of (S)-3-aminopyrrolidine. The product was analyzed with 99% chemical purity and 90% optical purity e.e.

References[1] Patent: US6348600, 2002, B1. Location in patent: Page column 14
[2] Patent: EP1640364, 2006, A1. Location in patent: Page/Page column 10
[3] Patent: EP1236716, 2002, A1. Location in patent: Example 6

(R)-3-Aminopyrrolidine Preparation Products And Raw materials

Raw materials(S)-(+)-1-Benzyl-3-aminopyrrolidine-->(S)-3-(Boc-amino)pyrrolidine-->Methanol-->Hydrogen
Preparation Products(R)-3-(Boc-amino)pyrrolidine
(R)-3-AMINOMETHYL-1-CBZ-PYRROLIDINE CAS 1217749-69-3
(R)-3-Hydroxy Myristic Acid CAS 28715-21-1
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