Hydrochloric Acid → HCID 70605606, compound

HRID 1112479Notes

Reaction equation

HRID 1112479 reaction equation
Cl[C:2]1[N:7]=[C:6]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])[N:5]=[C:4]([O:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33])[N:3]=1.[C:34]1([C:40]2[CH:46]=[C:45]([OH:47])[CH:44]=[C:43]([C:48]3[CH:53]=[CH:52][CH:51]=[CH:50][CH:49]=3)[C:41]=2[OH:42])[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1.[OH-].[Na+].Cl>O>[OH:42][C:41]1[C:40]([C:34]2[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=2)=[CH:46][C:45]([O:47][C:2]2[N:7]=[C:6]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])[N:5]=[C:4]([O:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH3:33])[N:3]=2)=[CH:44][C:43]=1[C:48]1[CH:49]=[CH:50][CH:51]=[CH:52][CH:53]=1

Participants

6

Reactant 4

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 5906441,3,5-Triazine, 2-chloro-4,6-bis(dodecyloxy)-HCID 10563427[1,1':3',1''-Terphenyl]-2',5'-diol

Product 1

HCID 70605606HCID 70605606, compound

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Procedure

In a 500 ml-three-necked flask 4.8 g (0.01 mole) of the 2-chloro-4,6-dilauroxy-s-triazine prepared above, were mixed with 2.6 g (0.01 mole) of 2,6-diphenyl hydroquinone. After rinsing with nitrogen, 150 ml of acetone were added, followied by adding dropwise, with vigorous stilling, 0.4 g (0.01 mole) of NaOH dissolved in 7 ml of water, at 20° C. The solution then assumed an orange-yellow color, which largely disappeared upon heating the reaction mixture for a longth of time under reflux. After completion of the reaction, the contents of the flask were poured into 100 ml of ice water containing 2 ml of hydrochloric acid. The organic layer was extracted three times with methylene chloride, after which the combined extracts were washed and dried. After concentration of the organic layer by evaporation a product was obtained which crystallized out after a length of time (melting point 18°-20° C).

Workup

  1. washAfter rinsing with nitrogen, 150 ml of acetone
  2. additionwere added
  3. temperatureupon heating the reaction mixture for a longth of time
  4. temperatureunder reflux
  5. customAfter completion of the reaction
  6. extractionThe organic layer was extracted three times with methylene chloride
  7. washafter which the combined extracts were washed
  8. customdried
  9. customAfter concentration of the organic layer by evaporation a product
  10. customwas obtained which
  11. customcrystallized out after a length of time (melting point 18°-20° C)

Sources & evidence

ORD record
ord-fb4e99e17c2d4b31bfc5f55521a541b3
Source dataset
uspto-grants-1978_10
Patent number
US04122270

Reaction notes

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