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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 254917Generated: October 31, 2026

Triethylamine → HCID 66890038, compound

https://huagongshe.com/reaction/254917

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN,N-Diethylethanamine trihydrofluorideHCID 175505—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 91092123HCID 91092123—
SolventMethanolHCID 887—
ProductHCID 66890038HCID 6689003890%

Reaction Steps

Compound 6 (110 g, 138.54 mmole) was dissolved in methanol (500 mL) and sodium methoxide (11 g, 204.0 mmole, 1.5 eq.) was added and the solution was stirred at room temperature for 2 hours. The reaction mixture was concentrated under reduced pressure, and the residue was partitioned between ether and water. The separated organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was dried in vacuo for 3 hrs and dissolved in dry THF under nitrogen. Triethylamine (TEA) (100 mL, 0.752 mole, 5 eq.) was added followed by triethylamine trihydrofluoride (TREAT.HF) (220 mL, 1.38 mole, 10 eq.) and the mixture was stirred overnight at room temperature. The solvent was removed under reduced pressure and the residue partitioned between ether and water. The ether layer was washed with brine and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure and the residue purified by flash chromatography (40% ethyl acetate in hexane) to give 51 g of compound 7 in 90% yield (reported literature yield 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07875733B2
Source datasetuspto-grants-2011_01
ORD IDord-0796d30a0acd48888cb7b194dcad19d7
Source noteuspto-grants-2011_01