Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613601Generated: October 30, 2026

Tetrabutylammonium Fluoride Trihydrate → 7-Nitro-trans-5-(5-chloro-1,2-dihydro-2-oxo-pyrid-1-yl)-2,3,4,5-tetrahydro-1-benzoxepin-4-ol

https://huagongshe.com/reaction/1613601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium Fluoride TrihydrateHCID 11726816—
Reactant4,5-Epoxy-7-nitro-2,3,4,5-tetrahydro-benzoxepinHCID 14580522—
Reactant5-Chloro-2-trimethylsilyl-pyridineHCID 15169006—
Product7-Nitro-trans-5-(5-chloro-1,2-dihydro-2-oxo-pyrid-1-yl)-2,3,4,5-tetrahydro-1-benzoxepin-4-olHCID 67883728—

Reaction Conditions

Temperature60 °C

Reaction Steps

6.63 g (21 mmol) of tetrabutylammonium fluoride trihydrate are added to a stirred mixture of 3.93 g (19 mmol) of 4,5-epoxy-7-nitro-2,3,4,5-tetrahydro-1-benzoxepin and 8.06 g (40 mmol) of 5-chloro-2-trimethylsilyl-pyridine, and the mixture is heated at 60° C. for 5 hours. The mixture is then stirred into ice-water and extracted several times with ethyl acetate. The combined ethyl acetate extracts are washed with water and saturated sodium chloride solution dried over sodium sulfate, filtered and evaporated in vacuo. The remaining viscous oil crystallizes after standing for some time. It is triturated with ethyl acetate and filtered off with suction. Crystals of melting point 219°-222° C. are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05194442
Source datasetuspto-grants-1993_03
ORD IDord-ec2cea65ada8406289989e264b095ac0
Source noteuspto-grants-1993_03