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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275212Generated: October 26, 2026

Sodium Azide → 1-Amino-2-(3,4-difluorophenyl)propan-2-ol

https://huagongshe.com/reaction/1275212

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant1-Azido-2-(3,4-difluorophenyl)-propan-2-olHCID 22993494—
Reactant2-(3,4-Difluorophenyl)-2-methyloxiraneHCID 22993508—
Reactant2-Azido-2-(3,4-difluorophenyl)-propan-1-olHCID 22993589—
ReactantLithium perchlorateHCID 23665649—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product1-Amino-2-(3,4-difluorophenyl)propan-2-olHCID 22993445—
Product2-Amino-2-(3,4-difluorophenyl)propan-1-olHCID 22993475—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-(3,4-difluorophenyl)-2-methyl-oxirane (1.2 g, 7.06 mmol) in 10 mL of acetonitrile was added sodium azide (0.69 g, 10.6 mmol) followed by lithium perchlorate (1.13 g, 10.6 mmol) and the suspension was heated to reflux overnight. After cooling, it was extraced with EtOAc, washed with saturated NaHCO3, dried over Na2SO4, filtered and the solvent was removed in vacuo. The light bron oil that was obtained was a 10:1 mixture of 1-azido-2-(3,4-difluorophenyl)-propan-2-ol and 2-azido-2-(3,4-difluorophenyl)-propan-1-ol (crude wt 2.0 g). It was dissolved in 40 mL of diethyl ether, cooled to 0° C. and then treated with a solution of lithium aluminum hydride (20.0 mL, 20 mmol). The resulting yellow suspension was then stirred at room temperature for 2 h. The reaction mixture was cooled to 0° C. and then carefully quenched sequentially with 0.8 mL of water, 0.8 mL of 3N NaOH followed by 2.5 mL of water. The resulting suspension was filtered thro' a fritted glass funnel. To the residue was added 100 mL Et2O and the suspension was heated to reflux for 20 min. The suspension was filtered and was combined with the previous filtrate, dried over MgSO4, filtered and the solvent was removed in vacuo. 1-Amino-2-(3,4-difluorophenyl)-propan-2-ol and 2-amino-2-(3,4-difluorophenyl)-propan-1-ol was obtained as a yellow glassy syrup (1.16 g, 87%) which was used in the next step immediately without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06159990
Source datasetuspto-grants-2000_12
ORD IDord-18ab77f341d7423aae7756a296267dfc
Source noteuspto-grants-2000_12