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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075325Generated: October 27, 2026

Sodium Azide → (2R,3R)-3-azido-3-(4-(trifluoromethyl)phenyl)propane-1,2-diol

https://huagongshe.com/reaction/2075325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AzideHCID 33557—
Reactant((2S,3S)-3-(4-(trifluoromethyl)phenyl)oxiran-2-yl)methanolHCID 12170819—
ReactantLithium perchlorateHCID 23665649—
SolventAcetonitrileHCID 6342—
Product(2R,3R)-3-azido-3-(4-(trifluoromethyl)phenyl)propane-1,2-diolHCID 8661377081%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a mixture of ((2S,3S)-3-(4-(trifluoromethyl)phenyl)oxiran-2-yl)methanol (15.00 g, 68.8 mmol) in 400 mL ACN was added lithium perchlorate (75.3 mL, 1719 mmol). The reaction mixture was a suspension. After stirring for 15 minutes, sodium azide (12.1 mL, 344 mmol) was added, and the mixture was heated at 65° C. for 24 hours under nitrogen. The reaction mixture was then cooled, and the solvent was evaporated under reduced pressure. Distilled water (500 mL) was added, and the resulting mixture was extracted 3 times (3×400 mL) with diethyl ether. The combined ether layers were directly dried over MgSO4. After removing the solvent, a colorless oil was obtained as the desired product (14.5 g, yield=81%). 1H NMR (400 MHz, CD3OD) δ ppm 3.50-3.56 (m, 1H) 3.58-3.63 (m, 1H) 3.84-3.90 (m, 1H) 4.78 (d, J=6.53 Hz, 1H) 7.62 (d, J=8.03 Hz, 2H) 7.67-7.73 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919504B2
Source datasetuspto-grants-2011_04
ORD IDord-6bd8ddc806b14b70a3dc18771c3d2c1e
Source noteuspto-grants-2011_04