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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007932Generated: October 30, 2026

Formamidine acetate → HCID 178521435, compound

https://huagongshe.com/reaction/1007932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormamidine acetateHCID 160693—
ReactantHCID 22666387HCID 22666387—
Solvent2-MethoxyethanolHCID 8019—
ProductHCID 178521435HCID 17852143556.6%

Reaction Steps

In 10 mL of ethylene glycol monomethyl ether is dissolved 1.2 g of 2-[(3,4-diaminophenethyl)oxy]-1-ethanol dihydrochloride, to which is added 0.93 g of formamidine acetate. The mixture is heated under reflux for 30 minutes. Then, the solvent is distilled off under reduced pressure, water and methylene chloride are added to the residue, pH is adjusted to 9 with 2 mol/L aqueous solution of sodium hydroxide, and the organic layer is separated. The aqueous layer is salted out and extracted with methylene chloride. The organic layers are collected, washed with saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. The solvent is distilled off under reduced pressure, and the residue is purified by column chromatography (eluent: chloroform:methanol=10:1) to obtain 0.52 g of 2-[2-(1H-benzo[d]imidazol-5-yl)ethoxy]-1-ethanol as an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06797726B1
Source datasetuspto-grants-2004_09
ORD IDord-971d8ef7305448beb46a8c6eb4f1f2fc
Source noteuspto-grants-2004_09