Hydrochloric Acid → HCID 70577204, compound
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]1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
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
- temperatureunder reflux for 22 hours
- temperatureThe mixture is cooled
- customthe ethanol is evaporated
- washThe residue is washed with ether, water (50 ml.)
- additionis added
- extractionThe alkaline solution is extracted with chloroform
- extractionthe chloroform extract
- washis washed with water
- dry with materialdried (MgSO4)
- customevaporated to dryness
- dissolutionThe gummy residue is dissolved in ethanol
- additiontreated with ethereal hydrochloric acid
- 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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