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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1451348Generated: October 30, 2026

N,N,N',N'-Tetramethylethylenediamine → HCID 53833864, compound

https://huagongshe.com/reaction/1451348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
Reactant1,1-DibromoethaneHCID 11201—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 3-furoateHCID 69201—
CatalystZincHCID 23994—
CatalystTitanium TetrachlorideHCID 24193—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53833864HCID 5383386454.3%

Reaction Steps

To 300 ml of THF was added with cooling (ice-bath) 300 ml (0.3 mol) of 1M TiCl4 in methylene chloride and the mixture was stirred for 10 min. To the above mixture was added at room temperature 90.5 ml (0.6 mol) of TMEDA, the mixture was stirred for 10 min, and then, 44.12 g (0.675 mol) of Zn dust was added with cooling to maintain the mixture at room temperature and stirred for 40 min. To the resulting reaction mixture was added dropwise a mixture of ethyl 3-furoate (10.5 g, 0.075 mol), 31 g (0.165 mol) of dibromoethane in 200 ml of THF, and the mixture was stirred at room temperature for 2.5 h. After adding 90 ml of aqueous potassium carbonate solution, the mixture was concentrated in vacuo, the residue was diluted with 20 g of basic alumina, passed through basic alumina column (ether/TEA 200:1), and the eluent was concentrated. The residue was triturated in ether (200 ml), filtered, and the filtrate was distilled (80°-95° C./25 mm) to afford 6.2 g of (54.3%) of 1-(3-furyl)-1-ethoxy-2-methylethylene (Formula III: R2 =CH3 ; R3 =H; R4 =CH3CH2O; R5 32 3-Furyl; and Formula III: R2 =H; R3 =CH3 ; R4 =3-Furyl; R5 =CH3CH2O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05604224
Source datasetuspto-grants-1997_02
ORD IDord-dc91205b0cf543b5a4494369dbd1b1b2
Source noteuspto-grants-1997_02