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Benzyl Chloride → HCID 21549820, compound

HRID 268160
Notes
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Reaction equation

HRID 268160 reaction equation
[NH2:1][CH2:2][C:3]1[CH:8]=[C:7]([CH3:9])[C:6]([CH2:10][NH2:11])=[CH:5][C:4]=1[CH3:12].[OH-].[Na+].[CH2:15](Cl)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>>[CH2:15]([NH:1][CH2:2][C:3]1[CH:8]=[C:7]([CH3:9])[C:6]([CH2:10][NH:11][CH2:2][C:3]2[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=2)=[CH:5][C:4]=1[CH3:12])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 3

HCID 7503Benzyl ChlorideHCID 14798Sodium HydroxideHCID 424357HCID 424357, compound

Product 1

HCID 21549820HCID 21549820, compound

Procedure

Separately, 32.8 parts of 1,4-diaminomethyl-2,5-dimethylbenzene and 100 parts of 20% caustic soda were heated at 80C. and reacted by adding 50.4 parts of benzyl chloride with stirring to obtain 50 parts of 1,4-bis(benzylaminomethyl)-2,5-dimethylbenzene, to which was then admixed 30 parts of octylphenoxyhexadecylethenoxyethylsulfate soda, 10 parts of a sperm oil alcohol-ethylene oxide adduct and 10 parts of isopropanol with stirring to obtain 100 parts of an emulsifier-incorporated composition.

Workup

  1. custom
and reacted

Sources & evidence

ORD record
ord-aa6a7108593649aeb990431c8115c734
Source dataset
uspto-grants-1976_03
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US03947389

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes