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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109740Generated: October 27, 2026

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

https://huagongshe.com/reaction/2109740

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 to 65° C. for 24 hours under nitrogen. After the reaction mixture was cooled, the solvent was evaporated under reduced pressure. 500 mL distilled water 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 numberUS07514566B2
Source datasetuspto-grants-2009_04
ORD IDord-492c2670c60245448c8c38ca64dffb5a
Source noteuspto-grants-2009_04