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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1012585Generated: October 31, 2026

Hydrochloric Acid → HCID 67314829, compound

https://huagongshe.com/reaction/1012585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 67314733HCID 67314733—
SolventEthanolHCID 702—
ProductHCID 67314829HCID 6731482998%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 50 ml recovery flask, 430 mg (0.867 mmol, 1.0 equivalent) of {(4-dipropylaminobutyl)-[4-(4-methoxybenzylidene)aminomethylbenzyl]}amino}ethyl acetate (30) was dissolved in 4.3 ml of ethanol. The solution was cooled to 0° C. After the dropwise addition of 4.3 ml of 2N hydrochloric acid over about five minutes, the mixture was stirred at 5° C. or less for 22 hours. The mixture was added with 4.3 ml of 2N hydrochloric acid at 0° C., stirred for three hours, and extracted five times with 25 ml of chloroform. The aqueous layer was slowly added with 50 ml of chloroform and 40 ml of a 3N sodium hydroxide aqueous solution to make the mixture basic, and the mixture was subjected to phase separation. The mixture was then extracted three times with 25 ml of chloroform. The extract was dried over anhydrous sodium sulfate, filtered, and concentrated, thereby obtaining 319 mg of [(4-aminomethylbenzyl)-(4-dipropylaminobutyl)amino]ethyl acetate (14) as a slightly yellow oily substance (yield: 98%). [HPLC: 95.9% (HPLC measurement conditions A)]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977512B2
Source datasetuspto-grants-2011_07
ORD IDord-80f9bd6e14fd45159585944a2e2b667a
Source noteuspto-grants-2011_07