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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644778Generated: October 31, 2026

p-Toluenesulfonyl azide → HCID 86641203, compound

https://huagongshe.com/reaction/1644778

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonyl azideHCID 13661—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantEthyl [3,5-bis(trifluoromethyl)phenyl]acetateHCID 42552891—
SolventAcetonitrileHCID 6342—
ProductHCID 86641203HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124633B2
Source datasetuspto-grants-2012_02
ORD IDord-8d12d6ee4c3c455b948b09345f05cd74
Source noteuspto-grants-2012_02