(+/-)-2-imino-1,4-dimethyl-3,3-diphenylpyrrolidine hydrochloride

Base Information

Chemical Name:(+/-)-2-imino-1,4-dimethyl-3,3-diphenylpyrrolidine hydrochloride
CAS No.:17268-75-6
Molecular Formula:C₁₈H₂₀N₂*ClH
Molecular Weight:300.831
Hs Code.:

Synonyms:

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Chemical Property of (+/-)-2-imino-1,4-dimethyl-3,3-diphenylpyrrolidine hydrochloride

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Technology Process of (+/-)-2-imino-1,4-dimethyl-3,3-diphenylpyrrolidine hydrochloride

There total 4 articles about (+/-)-2-imino-1,4-dimethyl-3,3-diphenylpyrrolidine hydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 87274-93-9
(+/-)-4-(N-carbomethoxy-N-methylamino)-2,2-diphenyl-3-methylbutyronitrile

: 17268-75-6
(+/-)-2-imino-1,4-dimethyl-3,3-diphenylpyrrolidine hydrochloride

Guidance literature:: With hydrogenchloride; hydrogen bromide; Yield given. Multistep reaction; 1.) glacial acetic acid, room temperature, 4 d, 2.) ether;
DOI:10.1002/jps.2600720627

Reference yield:

: 86-29-3
Diphenylacetonitrile

: 17268-75-6
(+/-)-2-imino-1,4-dimethyl-3,3-diphenylpyrrolidine hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) potassium tert-butoxide, 2.) sodium bicarbonate / 2.) chloroform, reflux, 24 h

2: 1.) hydrogen bromide, 2.) conc. hydrochloric acid / 1.) glacial acetic acid, room temperature, 4 d, 2.) ether

With hydrogenchloride; potassium tert-butylate; hydrogen bromide; sodium hydrogencarbonate;
DOI:10.1002/jps.2600720627

Reference yield:

: 108-14-5
2-chloro-1-dimethylaminopropane

: 17268-75-6
(+/-)-2-imino-1,4-dimethyl-3,3-diphenylpyrrolidine hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) potassium tert-butoxide, 2.) sodium bicarbonate / 2.) chloroform, reflux, 24 h

2: 1.) hydrogen bromide, 2.) conc. hydrochloric acid / 1.) glacial acetic acid, room temperature, 4 d, 2.) ether

With hydrogenchloride; potassium tert-butylate; hydrogen bromide; sodium hydrogencarbonate;
DOI:10.1002/jps.2600720627