Hydrochloric Acid → HCID 70577204, compound

HRID 1414567Notes

Reaction equation

HRID 1414567 reaction equation
O(C([N:10]1[CH2:15][CH2:14][C:13]2([C:28]3[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=3[O:22][C:21]3[C:16]2=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH2:12][CH2:11]1)=O)C1C=CC=CC=1.C(O)C.[OH-].[K+].[ClH:34]>O>[ClH:34].[NH:10]1[CH2:11][CH2:12][C:13]2([C:16]3[CH:17]=[CH:18][CH:19]=[CH:20][C:21]=3[O:22][C:23]3[C:28]2=[CH:27][CH:26]=[CH:25][CH:24]=3)[CH2:14][CH2:15]1

Participants

6

Procedure

A mixture of 1'-phenoxycarbonylxanthene-9-spiro-4'-piperidine (370 mg.), ethanol (80 ml.) and a 50% w/v solution of potassium hydroxide in water (20 ml.) is heated under reflux for 22 hours. The mixture is cooled and concentrated hydrochloric acid (20 ml.) is added and the ethanol is evaporated. The residue is washed with ether, water (50 ml.) is added and the resulting solution made alkaline with 3N sodium hydroxide. The alkaline solution is extracted with chloroform and the chloroform extract is washed with water, dried (MgSO4) and evaporated to dryness. The gummy residue is dissolved in ethanol and treated with ethereal hydrochloric acid. The solid is recrystallised from ethanol-ether to give xanthene-9-spiro-4'-piperidine hydrochloride, m.p. 248°-250° C.

Workup

  1. temperatureunder reflux for 22 hours
  2. temperatureThe mixture is cooled
  3. customthe ethanol is evaporated
  4. washThe residue is washed with ether, water (50 ml.)
  5. additionis added
  6. extractionThe alkaline solution is extracted with chloroform
  7. extractionthe chloroform extract
  8. washis washed with water
  9. dry with materialdried (MgSO4)
  10. customevaporated to dryness
  11. dissolutionThe gummy residue is dissolved in ethanol
  12. additiontreated with ethereal hydrochloric acid
  13. customThe solid is recrystallised from ethanol-ether

Sources & evidence

ORD record
ord-bf97a0820c284bbfa244e0020e211301
Source dataset
uspto-grants-1977_01
Patent number
US04001419

Reaction notes

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