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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 976245Generated: October 29, 2026

Triethylamine → HCID 21459900, compound

https://huagongshe.com/reaction/976245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 21459892HCID 21459892—
ReactantHCID 178418361HCID 178418361—
CatalystCobaltHCID 104730—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21459900HCID 2145990033.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of methyl 3-(cyanomethoxy)-5-methoxy-1-methyl-1H-indole-2-carboxylate (0.60 g, 2.2 mmol) and triethylamine (0.40 mL, 0.29 g, 2.9 mmol) in 35 mL of tetrahydrofuran in a pressure reaction vessel is treated with Raney cobalt catalyst (0.40 g). The reactor is pressurized with hydrogen (590 psi) and heated at 80° C. for 10 hours. The cooled reaction mixture is filtered and the filtrate evaporated. The oil residue is dissolved in 50 mL of methanol, and sodium methoxide (0.80 g, 15 mmol) is added to the solution. The mixture is heated at reflux for 3 hours, then cooled and evaporated. The residue is distributed between 75 mL of ethyl acetate and 150 mL of brine. The aqueous layer is extracted several times with fresh ethyl acetate. The combined organic layers are washed with brine, dried (anhydrous sodium sulfate) and evaporated. The crude product residue is purified by flash chromatography (silica gel, 5% methanol in dichloromethane elution) to yield 0.18 g (33%) of product. A sample recrystallized from ethyl acetatehexane has mp 184°-186° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05612330
Source datasetuspto-grants-1997_03
ORD IDord-91524d36dd534f23b72b71ccc0ef35e6
Source noteuspto-grants-1997_03