Benzaldehyde → HCID 86733767, compound

HRID 1439019Notes

Reaction equation

HRID 1439019 reaction equation
[CH2:1]([C:15]1[C:16]([CH2:23][OH:24])=[C:17]([OH:22])[C:18]([CH3:21])=[N:19][CH:20]=1)[S:2][S:3][CH2:4][C:5]1[C:6]([CH2:13][OH:14])=[C:7]([OH:12])[C:8]([CH3:11])=[N:9][CH:10]=1.[CH:25](=O)[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1.Cl>CCOCC>[CH2:4]([C:5]1[CH:10]=[N:9][C:8]([CH3:11])=[C:7]2[O:12][CH:25]([C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)[O:14][CH2:13][C:6]=12)[S:3][S:2][CH2:1][C:15]1[CH:20]=[N:19][C:18]([CH3:21])=[C:17]2[O:22][CH:25]([C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)[O:24][CH2:23][C:16]=12

Participants

5

Procedure

A mixture of 0.01 moles of 5,5'-(dithiodimethylene)bis[3-hydroxy-4-hydroxymethyl-2-methylpyridine] and 100 ml. of benzaldehyde was saturated with hydrogen chloride gas at 0°-5° and then stirred at this temperature for 4 hours. At this time 800 ml. of ether were added and the resulting precipitate was separated by filtration. This solid was then added to a well stirred mixture of 200 ml. chloroform and 200 ml. of water containing 20 gm. of sodium carbonate. After 15 minutes the chloroform layer was removed, dried, and concentrated to give an oil which gradually solidified. This solid was filtered with the aid of a small amount of ether to give 5,5'-(dithiodimethylene)bis[8-methyl-2-phenyl-4H-m-dioxino[4,5-c]pyridine].

Workup

  1. customthe resulting precipitate was separated by filtration
  2. additionThis solid was then added to a well
  3. stirringstirred
  4. additionmixture of 200 ml
  5. customAfter 15 minutes the chloroform layer was removed
  6. customdried
  7. concentrationconcentrated
  8. customto give an oil which
  9. filtrationThis solid was filtered with the aid of a small amount of ether

Sources & evidence

ORD record
ord-1ab33108ee7646649fbc3dbf44a3bcc4
Source dataset
uspto-grants-1977_11
Patent number
US04057637

Reaction notes

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