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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216656Generated: October 30, 2026

Triethylamine → HCID 68685133, compound

https://huagongshe.com/reaction/2216656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantGlycine methyl ester hydrochlorideHCID 122755—
ReactantSodium borohydrideHCID 4311764—
Reactant4-(2H-1,2,3-triazol-2-yl)benzaldehydeHCID 10797302—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68685133HCID 68685133—

Reaction Steps

To a solution of 60 g (347 mmol) of 4-[1,2,3]-triazol-2-yl-benzaldehyde in 1000 ml of CH2Cl2, 78.9 g (629 mmol) of glycine methylester hydrochloride, 104.2 ml (749 mmol) of triethylamine and 150 g of MgSO4 are successively added at 0–5° C. The mixture is stirred at r.t. for 18 h and filtered through celite. The filtrate is concentrated under reduced pressure and the residue is diluted with AcOEt. Et3N hydrochloride is filtered off and the filtrate is concentrated under reduced pressure in an azeotropic manner using toluene to give the crude imine. To a solution of the crude imine in 600 ml of THF and 600 ml of MeOH, 20 g (526 mmol) of NaBH4 is added portionwise at −20˜−10° C. and the mixture is stirred for 1 h. The reaction mixture is slowly quenched with sat. aqueous NH4Cl and then extracted with CH2Cl2. The combined extracts are washed with H2O, brine, dried over MgSO4 and concentrated under reduced pressure. The residue is purified by CC on silica gel (n-Hexane:AcOEt=2:1˜1:1) to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112611B2
Source datasetuspto-grants-2006_09
ORD IDord-48060b873d454f509fe2a775f4bd065a
Source noteuspto-grants-2006_09