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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium AzideHCID 33557—
ReactantMethanol--water (1/1)HCID 22242641—
ReactantN-Boc-3-pyrroline oxideHCID 86654475—
ProductTert-butyl (3R,4R)-3-azido-4-hydroxypyrrolidine-1-carboxylateHCID 15855750—

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08404866B2
Source datasetuspto-grants-2013_03
ORD IDord-00dc4db20ac4422faa3cc8048d52b095
Source noteuspto-grants-2013_03