(R)-3-Benzyloxy-Pyrrolidine Hydrochloride
(R)-3-Benzyloxy-Pyrrolidine Hydrochloride Basic information
- Product Name:
- (R)-3-Benzyloxy-Pyrrolidine Hydrochloride
- Synonyms:
-
- (R)-3-BENZYLOXY-PYRROLIDINE HYDROCHLORIDE
- (R)-3-Benzyloxy Pyrrolidine Hcl
- (3R)-3-(benzyloxy)pyrrolidine hydrochloride
- (3R)-3-benzyloxypyrrolidine
- 3-phenylmethoxypyrrolidine hydrochloride
- CAS:
- 927819-90-7
- MF:
- C11H16ClNO
- MW:
- 213.71
- Mol File:
- 927819-90-7.mol
(R)-3-Benzyloxy-Pyrrolidine Hydrochloride Chemical Properties
- storage temp.
- Sealed in dry,Room Temperature
(R)-3-Benzyloxy-Pyrrolidine Hydrochloride Usage And Synthesis
Uses
(R)-3-Benzyloxy-Pyrrolidine Hydrochloride is an important organic reagent that can be used as a building block for the synthesis of many organic compounds, such as (R)-ethyl 4-(3-(benzyloxy)pyrrolidin-1-yl)butanoate.
Synthesis
After N-tert-butoxycarbonyl-(R)-3-benzyloxypyrrolidine separately obtained was dissolved in isopropanol and heated to 40 °C, isopropanol solution of hydrogen chloride was dropped for 6 hours. After the reaction finished, the mixture was cooled to 23 °C and was concentrated to distil the solvent away. Further, ethyl acetate was added and the mixture was concentrated, thereby obtaining a concentrate in an amount of about. Then, the concentrate was heated to 40 °C, and isopropanol was added until (R)-3-benzyloxypyrrolidine hydrochloride which had been separated as an oily substance became completely dissolved. After (R) -3-benzyloxypyrrolidine hydrochloride was crystallized by gradually cooling the solution and suitably adding a seed crystal, hexane was further added. At the time, crystallization solvent was in a following proportion: isopropanol/ethyl acetate/hexane = 1/71.5/71.5. A deposited crystal was subjected to filtration under reduced pressure, and the resultant wet crystal was washed with ethyl acetate, and then a wet crystal was dried under reduced pressure, thereby obtaining dry crystal of (R)-3-benzyloxypyrrolidine hydrochloride (yield of 82 %, purity of 99.8 %).
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