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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196281Generated: October 29, 2026

Ammonium Chloride → (S)-1-Azido-2-(5-bromo-2-fluoro-phenyl)-propan-2-ol

https://huagongshe.com/reaction/2196281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant18-Crown-6HCID 28557—
ReactantSodium AzideHCID 33557—
Reactant(S)-2-(5-Bromo-2-fluoro-phenyl)-2-methyl-oxiraneHCID 86650263—
SolventEthanolHCID 702—
Product(S)-1-Azido-2-(5-bromo-2-fluoro-phenyl)-propan-2-olHCID 86650264—

Reaction Steps

To a solution of (S)-2-(5-bromo-2-fluoro-phenyl)-2-methyl-oxirane (51.85 g, 224 mmol) in EtOH (800 ml) was added NaN3 (36.8 g, 531 mmol), NH4Cl (60.6 g, 1122 mmol) and 18-crown-6 (59.8 g, 224 mmol) and the reaction mixture was heated at reflux for 6 h. The reaction mixture was filtered and concentrated to half of its volume. The residual oil was extracted with EtOAc. Combined extracts were washed with saturated NaHCO3 solution and brine, dried over MgSO4, filtered and concentrated to provide the title compound as a light yellow oil: TLC (hexane-EtOAc 1:1): Rf=0.70; UPLC RtH3=1.115 min; 1H NMR (360 MHz, CDCl3): δ 7.72 (dd, 1H), 7.32 (m, 1H), 6.85 (dd, 1H), 3.73 (d, 1H), 3.51 (d, 1H), 2.44 (s, 1H), 1.50 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338413B1
Source datasetuspto-grants-2012_12
ORD IDord-cacf19ee58224577b38688cb47a8883d
Source noteuspto-grants-2012_12