Pyridine → HCID 12953546, compound

HRID 2285773Notes

Reaction equation

HRID 2285773 reaction equation
[C:1]1([C:7]2([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)[CH:11]([CH2:12]O)[CH2:10][N:9]([CH:14]([CH3:16])[CH3:15])[C:8]2=[O:17])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(Cl)([Cl:26])=O.N1C=CC=CC=1.[OH-].[Na+]>C(Cl)(Cl)Cl>[Cl:26][CH2:12][CH:11]1[CH2:10][N:9]([CH:14]([CH3:16])[CH3:15])[C:8](=[O:17])[C:7]1([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

6

Procedure

A solution of 43 g. (0.14 mole) of 3,3-diphenyl-4-hydroxymethyl-1-isopropyl-2-pyrrolidinone in 250 ml. of chloroform was treated with 33 g. (0.28 mole) of thionyl chloride over a one minute period followed by the dropwise addition of 22 g. (0.23 mole) of pyridine over a 30 minute period. The mixture was refluxed 18 hours and then poured onto ice. The cold mixture was made basic by the addition of sodium hydroxide. The chloroform layer was separated, dried over sodium sulfate and concentrated. The residue was crystallized using charcoal from a 25% ethyl acetate--75% isopropyl ether mixture. The crystalline solid was recrystallized from a 75% ethanol--25% water mixture and then from isopropyl ether. The dried 4-chloromethyl-3,3-diphenyl-1-isopropyl-2-pyrrolidinone weighed 23 g. and melted at 114°-116° C.

Workup

  1. temperatureThe mixture was refluxed 18 hours
  2. additionpoured onto ice
  3. customThe chloroform layer was separated
  4. dry with materialdried over sodium sulfate
  5. concentrationconcentrated
  6. customThe residue was crystallized
  7. customThe crystalline solid was recrystallized from a 75% ethanol--25% water mixture

Sources & evidence

ORD record
ord-4d0161bc7b914d2ba9756c833aa2245f
Source dataset
uspto-grants-1982_04
Patent number
US04324791

Reaction notes

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