Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 15766659 | HCID 15766659 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18956271 | HCID 18956271 | 47% |
Reaction Steps
To a stirred solution of 1.0 g (3.25 mmols) of 2-(4-chlorophenyl)-2-[(1,2,4-triazol-1-yl)methyl]hexanoic acid in 3 mL of dimethylformamide was added 0.30 mL of tert-butanol. This solution was cooled to 0° C. and a solution of 1.07 g (3.90 mmols) of diphenylphosphorylazide in 1 mL of dimethylformamide was added followed by 0.72 mL (7.15 mmols) of triethylamine. The resultant mixture was stirred for 2 hours and then allowed to warm to room temperature and stirred for an additional 15 hours. Addition of ice caused the precipitation of the product. Filtration gave 1.10 g of a crude product which was carefully recrystallized from a 1 to 3 mixture of ethyl acetate and hexane to afford 0.46 g (47%) of azide as a white crystalline solid, melting point 100°-101° C.: 1H-NMR (CDCl3, Me4Si) 0.7-1.1 (t, J=6 Hz, CH2 --CH3), 1.1-1.7 (m), 1.75-2.1 (m), 4.6 (d, CH2 --N), 6.8-7.2(m,phenyl H), 7.3 (s,CH=N), 7.7 ppm (s,CH=N):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05252594 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-b5221620f4454eeea7814d93748c37b4 |
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| Source note | uspto-grants-1993_10 |
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