HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952428Generated: October 26, 2026
Ammonium Chloride → Tert-butyl (3R,4R)-3-azido-4-hydroxypyrrolidine-1-carboxylate
https://huagongshe.com/reaction/1952428
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | Methanol--water (1/1) | HCID 22242641 | — |
| Reactant | N-Boc-3-pyrroline oxide | HCID 86654475 | — |
| Product | Tert-butyl (3R,4R)-3-azido-4-hydroxypyrrolidine-1-carboxylate | HCID 15855750 | — |
Reaction Steps
A mixture of N-Boc-3-pyrroline oxide (0.925 g, 5.0 mmol), NaN3 (0.65 g, 10 mmol), and NH4Cl (5.0 mmol) in MeOH—H2O (6:1, 16 mL) was stirred at 65° C. overnight. The reaction mixture was concentrated under reduced pressure and the residue was extracted thoroughly with ethyl acetate. The combined ethyl acetate extract was washed with water and sat. brine, dried over anhydrous Na2SO4, and evaporated. The crude azidoalcohol was purified by recrystallization from ether-hexane: mp 34-36° C.; 1H NMR (300 MHz, CD3OD) δ 4.16 (m, 1H), 3.95 (m, 1H), 3.62 (m, 1H), 3.51 (m, 1H), 3.35 (m, 2H), 1.47 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08404866B2 |
|---|
| Source dataset | uspto-grants-2013_03 |
|---|
| ORD ID | ord-00dc4db20ac4422faa3cc8048d52b095 |
|---|
| Source note | uspto-grants-2013_03 |
|---|