Potassium Iodide → HCID 12340297, compound

HRID 1578658Notes

Reaction equation

HRID 1578658 reaction equation
[NH:1]1[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[Cl:7][CH2:8][C:9]([C:11]1[CH:24]=[CH:23][C:22]2[O:21][C:20]3[C:15](=[CH:16][C:17]([C:25](=[O:28])[CH2:26]Cl)=[CH:18][CH:19]=3)[CH2:14][C:13]=2[CH:12]=1)=[O:10].[I-].[K+]>O1CCCC1>[ClH:7].[ClH:7].[N:1]1([CH2:8][C:9]([C:11]2[CH:24]=[CH:23][C:22]3[O:21][C:20]4[C:15](=[CH:16][C:17]([C:25](=[O:28])[CH2:26][N:1]5[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]5)=[CH:18][CH:19]=4)[CH2:14][C:13]=3[CH:12]=2)=[O:10])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1

Participants

5

Procedure

To a solution of 200 ml of piperidine in 500 ml of tetrahydrofuran are added 33.5 g (0.1 mole) of 2,7-bis(2-chloroacetyl)xanthene and 2g of potassium iodide with warming. The reaction mixture is allowed to stand for 7 days, filtered and the filtrate evaporated to dryness, leaving a residue which is treated with dilute acid and filtered. The filtrate is made alkaline, and the resulting oily product is extracted with methylene chloride. The methylene chloride solution is acidified with ethereal HCl which gives an oily product that is recrystallized from methanol-diethyl ether then vacuum dried to give 2,7-bis(piperidinoacetyl)xanthene dihydrochloride, M.P. 260°-262°C.

Workup

  1. temperaturewith warming
  2. filtrationfiltered
  3. customthe filtrate evaporated to dryness
  4. customleaving a residue which
  5. additionis treated
  6. additionwith dilute acid
  7. filtrationfiltered
  8. extractionthe resulting oily product is extracted with methylene chloride
  9. customgives an oily product that
  10. customis recrystallized from methanol-diethyl ether
  11. customvacuum dried

Sources & evidence

ORD record
ord-b4eb89921ea94e4f93134b9256e565a9
Source dataset
uspto-grants-1976_02
Patent number
US03937833

Reaction notes

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