HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonyl azide → HCID 86641203, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonyl azide | HCID 13661 | — |
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Ethyl [3,5-bis(trifluoromethyl)phenyl]acetate | HCID 42552891 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86641203 | HCID 86641203 | — |
Reaction Steps
To a solution of ethyl 3,5-bis(trifluoromethyl)phenylacetate (Step M, 26.0 g, 87 mmol) and 4-methylbenzenesulfonyl azide (Step L, 18.0 g, 91 mmol) in dry acetonitrile (150 mL) was added DBU (14.3 mL, 95 mmol) dropwise at −10° C. over 15 min with stirring. The mixture was stirred at −10° C. for a further 0.5 hr. The solvent was removed and the residue was partitioned between ether and water. The organic layer was washed with aqueous NaHCO3, brine, dried over Mg2SO4, and the solvent was removed. The residue was chromatographed (eluted with 9:1 hexane:ethyl acetate) to afforded a yellow solid. 1H-NMR (CDCl3): δ: 8.0 (2H, s), 7.68 (1H, s), 4.41 (2H, d, J=7.1 Hz), 1.40 (3H, t, J=7.1 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08124633B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-8d12d6ee4c3c455b948b09345f05cd74 |
| Source note | uspto-grants-2012_02 |