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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763557Generated: November 1, 2026

2,2-Diethoxyethylamine → HCID 178467951, compound

https://huagongshe.com/reaction/1763557

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2-DiethoxyethylamineHCID 69524—
ReactantHCID 178504055HCID 178504055—
ProductHCID 178467951HCID 178467951—

Reaction Steps

6 g of 1-(5-chlorindolin-1yl)-2-methylisothiourea hydrochloride and 10 ml of aminoacetaldehyde diethyl acetal were heated to a bath temperature of 120° for 1 hour. The excess aminoacetaldehyde diethyl acetal was removed by evaporation in a vacuum and the evaporation residue was partitioned between ethyl acetate and 1N aqueous sodium hydroxide solution. The organic phase was dried over magnesium sulphate and was evaporated to dryness. The 1-(5-chloroindolin-1-yl)-3-(2,2-diethoxyethyl)guanidine obtained as the evaporation residue was crystallized as the naphthalene-1,5-disulphonate having a M.Pt. of 163° -165° (from ethanol/ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04112111
Source datasetuspto-grants-1978_09
ORD IDord-1ffd67128c2f432eb8667028fce3500a
Source noteuspto-grants-1978_09