Chlorosuccinimide → HCID 70579239, compound

HRID 2286912Notes

Reaction equation

HRID 2286912 reaction equation
[ClH:1].[CH3:2][N:3]1[CH2:8][CH2:7][C:6]2([C:21]3[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=3[O:15][C:14]3[C:9]2=[CH:10][CH:11]=[CH:12][CH:13]=3)[CH2:5][CH2:4]1.[Cl:22]N1C(=O)CCC1=O>ClCCl>[ClH:22].[Cl:1][C:11]1[CH:12]=[CH:13][C:14]2[O:15][C:16]3[C:21]([C:6]4([CH2:7][CH2:8][N:3]([CH3:2])[CH2:4][CH2:5]4)[C:9]=2[CH:10]=1)=[CH:20][C:19]([Cl:22])=[CH:18][CH:17]=3

Participants

4

Procedure

A mixture of 1'-methylxanthene-9-spiro-4'-piperidine hydrochloride (5 g.), N-chlorosuccinimide (4.5 g.) and dichloromethane (100 ml.) is refluxed for 72 hours. The solution is washed with saturated sodium bicarbonate solution then water and dried with MgSO4. The solution is evaporated to give a gummy residue which is chromatographed on grade 3 aluminium oxide, Woelm basic. The product is eluted with 30% petroleum-ether (b.p. 60°-80° C.)/chloroform, taken up in ether and the solution treated with ethereal hydrochloric acid. The precipitate is filtered and recrystallised from ethanol-ether to give 2,7-dichloro-1'-methylxanthene-9-spiro-4'-piperidine hydrochloride, m.p. 285° C.

Workup

  1. temperatureis refluxed for 72 hours
  2. washThe solution is washed with saturated sodium bicarbonate solution
  3. dry with materialwater and dried with MgSO4
  4. customThe solution is evaporated
  5. customto give a gummy residue which
  6. customis chromatographed on grade 3 aluminium oxide, Woelm basic
  7. washThe product is eluted with 30% petroleum-ether (b.p. 60°-80° C.)/chloroform
  8. additionthe solution treated with ethereal hydrochloric acid
  9. filtrationThe precipitate is filtered
  10. customrecrystallised from ethanol-ether

Sources & evidence

ORD record
ord-ec9839929f2e4dc78db2a17bff6a5577
Source dataset
uspto-grants-1981_05
Patent number
US04268514

Reaction notes

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