HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007932Generated: October 30, 2026
Formamidine acetate → HCID 178521435, compound
https://huagongshe.com/reaction/1007932
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formamidine acetate | HCID 160693 | — |
| Reactant | HCID 22666387 | HCID 22666387 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | HCID 178521435 | HCID 178521435 | 56.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06797726B1 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-971d8ef7305448beb46a8c6eb4f1f2fc |
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| Source note | uspto-grants-2004_09 |
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