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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801736Generated: October 30, 2026

Isoamyl Nitrite → HCID 66650354, compound

https://huagongshe.com/reaction/1801736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsoamyl NitriteHCID 8053—
ReactantAmino-5-ethoxy-4-trifluoromethyl-benzonitrileHCID 66650419—
SolventTetrahydrofuranHCID 8028—
SolventSodium BicarbonateHCID 516892—
ProductHCID 66650354HCID 6665035485%

Reaction Steps

To a solution of 2-amino-5-ethoxy-4-trifluoromethyl-benzonitrile from step 4 (31.62 g, 137.4 mmol) in dry THF (410 mL) was added isoamyl nitrite (40.4 mL, 302 mmol) and the mixture was refluxed for 16 h. The solvent was removed in vacuum to give an orange oil, which was dissolved in sat. NaHCO3-sol., extracted three times with diethyl ether. The combined organic layers were washed with 1 N HCl and brine, dried over Na2SO4. Removal of the solvent in vacuum left an orange oil, which was purified by double Kugelrohr distillation (up to 160° C. bath temperature at 1.5 mbar) to give the title compound as a light yellow solid (25.06 g, 85%). MS (EI) 185.1 [M].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349844B2
Source datasetuspto-grants-2013_01
ORD IDord-03d49d767d424f9292fdde1513245b2d
Source noteuspto-grants-2013_01