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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218859Generated: October 26, 2026

Sodium Bicarbonate → HCID 23142789, compound

https://huagongshe.com/reaction/2218859

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantBis(2-chloroethyl)amine hydrochlorideHCID 522769—
Reactant4-Methoxy-2-(3,3,5,5-tetramethylcyclohexyl)phenylamineHCID 23142124—
Solvent1,2-DichlorobenzeneHCID 7239—
ProductHCID 23142789HCID 23142789—

Reaction Conditions

Temperature220 °C

Reaction Steps

A mixture of the crude product of 4-methoxy-2-(3,3,5,5-tetramethylcyclohexyl)phenylamine produced in Example (85b), bis(2-chloroethyl)amine hydrochloride (770 mg, 4.33 mmol) and 1,2-dichlorobenzene (10 ml) was stirred for 2 hours at an external temperature of 220° C. During the reaction, the excess hydrogen chloride gas in the reactor was removed several times with nitrogen gas. Bis(2-chloroethyl)amine hydrochloride (180 mg, 1.01 mmol) was then added and the mixture was stirred for 1 hour under the same conditions. The reaction mixture was cooled to room temperature, saturated aqueous solution of sodium hydrogencarbonate was added and extraction was performed with chloroform. The aqueous layer was again extracted with chloroform, and the organic layers were combined, washed with brine and then dried over anhydrous magnesium sulfate. The desiccant was filtered off and the filtrate was concentrated under reduced pressure. The resultant residue was purified by NH silica gel column chromatography (ethyl acetate/heptane) to give 660 mg of the title compound as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07410971B2
Source datasetuspto-grants-2008_08
ORD IDord-681824e9b1ed474ba7c79cfbe917f57b
Source noteuspto-grants-2008_08