Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (S)-1-Benzyl-3-mesyloxypyrrolidine | HCID 10934081 | — |
| Product | (3R)-1-benzylpyrrolidin-3-amine | HCID 1519354 | 73% |
Reaction Steps
In an autoclave were charged 5.303 g of (S)-1-benzyl-3-(methanesulfonyloxy)pyrrolidine (20 mmol, optical purity: 100% e.e.), and 42.53 g of 40% by weight aqueous ammonia (50 equivalent), which was heated to 80° C. whereby an internal pressure of 8 barr was observed. After allowing the reaction for 20 hrs, the reaction mixture was cooled to room temperature, followed by addition of 4.00 g of a 30% by weight aqueous sodium hydroxide solution (1.5 equivalent), and then ammonia was removed by distillation under reduced pressure. The residue was extracted with 30 mL of ethyl acetate three times, and the organic layers were combined. After washing with 3 mL of a saturated brine, drying over anhydrous magnesium sulfate, and concentration under reduced pressure gave 3.6146 g of a dark red oily material (reaction yield: 73%, optical purity: 92.4% e.e.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08030501B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-6b24a42dd3ff40dba884c0c4a87c9856 |
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| Source note | uspto-grants-2011_10 |
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