Hydrochloric Acid → HCID 19819765, compound

HRID 1031175Notes

Reaction equation

HRID 1031175 reaction equation
Cl.[C:2]([N:6]1[CH2:10][CH2:9][CH:8](O)[CH2:7]1)([CH3:5])([CH3:4])[CH3:3].S(Cl)([Cl:14])=O>C(Cl)(Cl)Cl>[Cl:14][CH:8]1[CH2:9][CH2:10][N:6]([C:2]([CH3:5])([CH3:4])[CH3:3])[CH2:7]1

Participants

5

Procedure

Hydrogen chloride gas was bubbled into a solution of 1-t-butyl-3-pyrrolidinol (146 g, 1.02 mol) in chloroform (1.01) until the reaction mixture became acidic. A solution of thionyl chloride (1.55 g, 1.3 mol) was added dropwise with warming. After the addition was completed, the reaction mixture was stirred at reflux temperature for 18 h. The chloroform and excess thionyl chloride was removed on a rotary evaporator. Cracked ice and water was added to the residue and the mixture basified with 25% sodium hydroxide solution. The mixture was extracted with chloroform, and the extract washed with brine solution. The extract was dried (Na2SO4), concentrated and distilled at 75° C./15 mm to obtain 104 g (63%) of the title compound.

Workup

  1. temperaturewith warming
  2. additionAfter the addition
  3. temperatureat reflux temperature for 18 h
  4. customThe chloroform and excess thionyl chloride was removed on a rotary evaporator
  5. additionCracked ice and water was added to the residue
  6. extractionThe mixture was extracted with chloroform
  7. washthe extract washed with brine solution
  8. dry with materialThe extract was dried (Na2SO4)
  9. concentrationconcentrated
  10. distillationdistilled at 75° C./15 mm

Sources & evidence

ORD record
ord-2fdce3510fa54dd998014ec366a7db1b
Source dataset
uspto-grants-1992_04
Patent number
US05109013

Reaction notes

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