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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670641Generated: October 30, 2026

Tetrahydrofuran → HCID 57748783, compound

https://huagongshe.com/reaction/1670641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 67335783HCID 67335783—
ReactantHCID 67335785HCID 67335785—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 57748783HCID 57748783118.3%

Reaction Steps

Purge with nitrogen for five min a mixture of (4-bromo-2-nitro-phenyl)-(1-methyl-azetidin-3-yl)-amine (709 μmol, 203 mg), (E)-3,7-difluoro-11-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-ylmethylene)-6,11-dihydro-dibenzo[b,e]oxepine (723 μmol, 268 mg) in methanol (1.0 mL)/tetrahydrofuran (3.0 mL) (1:3 solvent ratio) in a sealed tube. Add sodium methoxide (1.42 mmol, 77 mg), tetrakis(triphenylphosphine)palladium (35 μmol, 41 mg) and heat at 70° C. overnight. Dilute with ethyl acetate, wash with 10% sodium bicarbonate twice, dry over anhydrous sodium sulfate, filter, and concentrate in vacuo to obtain 377 mg of an orange oil residue. Purify on a 12 g silica gel column eluting with 5% methanol in dichloromethane to obtain the title compound (199 mg, 62%). LC-MS m/z 450.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994164B2
Source datasetuspto-grants-2011_08
ORD IDord-14a819f46b5742628a8ff054ddb6c413
Source noteuspto-grants-2011_08