HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2280380Generated: November 5, 2026
Water → (3R,4R)-1-Boc-3-amino-4-fluoropyrrolidine
https://huagongshe.com/reaction/2280380
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | trans-Tert-butyl 3-azido-4-fluoropyrrolidine-1-carboxylate | HCID 118081950 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3R,4R)-1-Boc-3-amino-4-fluoropyrrolidine | HCID 72207654 | — |
Reaction Steps
In a round-bottomed flask equipped with a magnetic stir bar and a reflux condenser, to a solution of trans-tert-butyl 3-azido-4-fluoropyrrolidine-1-carboxylate (45 mg, 0.195 mmol) in THF (2.5 mL) was added PPh3 on polystyrene (1.6 mmol/g, 120 mg, 0.193 mmol) and water (0.15 mL). The reaction mixture was stirred at 60° C. for 2 h. The mixture was then filtered and the filtrate dried over MgSO4 and filtered. The solvent was removed under reduced pressure to afford trans-tert-butyl 3-amino-4-fluoropyrrolidine-1-carboxylate as a pale yellow oil. LC-MS-conditions 10: tR=0.48 min; [M-CH3+H]+=190.38.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09139524B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-5b2062696ae04aa483dc1a3193e5389c |
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| Source note | uspto-grants-2015_09 |
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