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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259425Generated: November 3, 2026

Diethyl Ether → HCID 178441886, compound

https://huagongshe.com/reaction/2259425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantLithium BromideHCID 82050—
ReactantMethyl 3-oxoheptanoateHCID 546075—
ReactantPotassiumHCID 5462222—
ReactantHCID 10794130HCID 10794130—
Reactant5-[4-(Bromomethyl)[1,1′-biphenyl]-2-yl]-1-(triphenylmethyl)-1H-tetrazoleHCID 18936121—
SolventDimethylformamideHCID 6228—
ProductHCID 178441886HCID 178441886—

Reaction Steps

methyl 3-oxo-2-[[2'-(1-triphenylmethyl-1H-tetrazol-5yl)[1,1'-biphenyl]-4-yl]methyl]heptanoate. To a solution of 0.97 g of potassium 1,1-dimethylethylate in 15 ml of dimethylformamide, chilled on an ice bath, under an atmosphere of argon, a solution of 1.3 g of methyl 3-oxoheptanoate in 13 ml of dimethylformamide is added, followed by 1.67 g of lithium bromide and a solution of 5 g of 5-[4-(bromomethyl)[1,1'-biphenyl]-2-yl]-1-triphenylmethyl-1H-tetrazole in 25 ml of dimethylformamide. The reaction mixture is stirred for 5 hours at room temperature and then diluted with 300 ml of ether. The mixture is washed twice with 100 ml of water and then with 100 ml of a saturated aqueous solution of ammonium chloride. It is dried on magnesium sulfate and evaporated in vacuo to obtain 4.6 g of the product in the form of a yellow oil used as such in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05472967
Source datasetuspto-grants-1995_12
ORD IDord-841dc951d2dc42d09fdb00334eaf7c5c
Source noteuspto-grants-1995_12