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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | ((2S,3S)-3-(4-(trifluoromethyl)phenyl)oxiran-2-yl)methanol | HCID 12170819 | — |
| Reactant | Lithium perchlorate | HCID 23665649 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (2R,3R)-3-azido-3-(4-(trifluoromethyl)phenyl)propane-1,2-diol | HCID 86613770 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07919504B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-6bd8ddc806b14b70a3dc18771c3d2c1e |
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| Source note | uspto-grants-2011_04 |
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