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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671344Generated: October 31, 2026

Diethyl Ether → HCID 67212560, compound

https://huagongshe.com/reaction/1671344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantNitronium tetrafluoroborateHCID 11073463—
Reactant3-(2,4-Dichloro-phenyl)-2,6-dimethyl-pyrazolo[5,1-b]oxazoleHCID 59186007—
SolventAcetonitrileHCID 6342—
ProductHCID 67212560HCID 67212560—

Reaction Steps

To a solution of 3-(2,4-dichloro-phenyl)-2,6-dimethyl-pyrazolo[5,1-b]oxazole (Intermediate HE) (768 mg, 2.73 mmol) in MeCN (13 ml) is added nitronium tetrafluoroborate (0.5M solution in sulfolane, 6.6 ml, 3.3 mmol, 1.2 eq.). The dark orange reaction mixture is stirred at RT for 3 h then diluted into Et2O (150 ml) and washed successively with Na2CO3 1M in water (100 ml), water (100 ml) and brine (50 ml). The organic layer is dried over Na2SO4, filtered and concentrated to dryness under reduced pressure. The resulting crude residue is purified by Combi-Flash Companion™ (Isco Inc.) column chromatography (SiO2; gradient elution, heptane/TBME 95:5→7:3) to yield the title compound as a greenish solid. TLC: RF=0.27 (heptane/TBME 3:1); HPLC: AtRet=2.73; MS: m/z 325.8 [M+H]+; 1H NMR (400 MHz, CDCl3) δ 2.49 (s, 3H), 2.66 (s, 3H), 7.47 (dd, J 8.3, 2.0, 1H), 7.52 (d, J 8.3, 1H), 7.64 (d, J 2.0, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994203B2
Source datasetuspto-grants-2011_08
ORD IDord-e39d3d05480e43fcb6ac668a2c9fde19
Source noteuspto-grants-2011_08