Toluene → N-(p-Bromobenzyl)-N-(4-methoxyphenyl)hydrazine hydrochloride

HRID 2366091Notes

Reaction equation

HRID 2366091 reaction equation
[ClH:1].[CH3:2][O:3][C:4]1[CH:9]=[CH:8][C:7]([NH:10][NH2:11])=[CH:6][CH:5]=1.C1(C)C=CC=CC=1.[Br:19][C:20]1[CH:27]=[CH:26][C:23]([CH2:24]Br)=[CH:22][CH:21]=1.CCN(CC)CC>C(OCC)(=O)C>[ClH:1].[Br:19][C:20]1[CH:27]=[CH:26][C:23]([CH2:24][N:10]([C:7]2[CH:8]=[CH:9][C:4]([O:3][CH3:2])=[CH:5][CH:6]=2)[NH2:11])=[CH:22][CH:21]=1

Participants

6

Conditions

Temperature
102.5 °C

Procedure

4-Methoxyphenyl hydrazine hydrochloride (1.0 eq) was added to a reaction flask containing of toluene (16 eq.; V/W of starting material) under nitrogen. To this reaction flask was added 4-bromo-benzylbromide (1.05 eq) and Et3N (2.1 eq). The reaction mixture was heated to about 100-105° C. and stirred for about 3 hours after which the reaction flask was cooled to room temperature. Ethyl acetate (10.0-fold, V/W of starting material) was added to the reaction flask and agitated for about 1.5 hours. The reaction mixture was filtered to collect the solid which was subsequently washed with toluene and dried in vacuo. Ethyl acetate was then added and the solution was agitated. The pH of the mixture was adjusted to a pH of 2 with saturated HO/Ethyl acetate solution and further agitated for 1 hour. The solid was then collected and washed with ethyl acetate and then air dried. The product was taken on to the next step without further purification.

Workup

  1. temperaturewas cooled to room temperature
  2. stirringagitated for about 1.5 hours
  3. filtrationThe reaction mixture was filtered
  4. customto collect the solid which
  5. washwas subsequently washed with toluene
  6. customdried in vacuo
  7. additionEthyl acetate was then added
  8. stirringthe solution was agitated
  9. stirringfurther agitated for 1 hour
  10. customThe solid was then collected
  11. washwashed with ethyl acetate
  12. customair dried
  13. customThe product was taken on to the next step without further purification

Sources & evidence

ORD record
ord-a4d3b934f3be45efb7adb5de182dea50
Source dataset
uspto-grants-2014_04
Patent number
US08697730B2

Reaction notes

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