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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253368Generated: November 2, 2026

N-Benzylnormechlorethamine → 2,2'-((Phenylmethyl)imino)bisethanol

https://huagongshe.com/reaction/1253368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-BenzylnormechlorethamineHCID 5928—
ReactantBenzyl ChlorideHCID 7503—
ReactantDiethanolamineHCID 8113—
Product2,2'-((Phenylmethyl)imino)bisethanolHCID 7553—

Reaction Steps

In the process for preparing N,N-bis(2-chloroethyl)benzylamine by first reacting benzyl chloride with N,N-bis(2-hydroxyethyl)amine to produce N,N-bis(2-hydroxyethyl)benzylamine and then reacting N,N-bis(2-hydroxyethyl)benzylamine with thionvl chloride to produce N,N-bis(2-chloroethyl)benzylamine, the improvements which comprise adding about one molar equivalent of benzyl chloride to a warmed mixture containing about one molar equivalent of N,N-bis(2-hydroxyethyl)amine and about one molar equivalent of sodium carbonate, the addition rate of benzyl chloride being so as to maintain the exothermic reaction temperature at about 70° to 100° C.; maintaining the reaction temperature at about 70° to 100° C. for a short period; adding toluene to the reaction mixture; separating and drying the toluene solution containing N,N-bis(2-hydroxyethyl)benzylamine; adding said dry toluene solution to more than two molar equivalents of thionyl chloride heated to about 65°-75° C., the rate of addition being so as to maintain the reaction temperature at about 65°-75° C.; treating the reaction mixture with aqueous alkali; and, separating the toluene solution containing a substantially quantitative yield of the N,N-bis(2-chloroethyl)benzylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04748276
Source datasetuspto-grants-1988_05
ORD IDord-373f497a4aea4c5e840e560ecc535909
Source noteuspto-grants-1988_05