Hydrochloric Acid → p-Toluenesulfonic acid

HRID 217269Notes

Reaction equation

HRID 217269 reaction equation
Cl.O.[OH-].[Na+].O.[C:6]1([CH3:16])[CH:11]=[CH:10][C:9]([S:12]([OH:15])(=[O:14])=[O:13])=[CH:8][CH:7]=1>CC(OC)(C)C.CCCCCCC>[CH3:16][C:6]1[CH:11]=[CH:10][C:9]([S:12]([OH:15])(=[O:14])=[O:13])=[CH:8][CH:7]=1

Participants

7

Conditions

Temperature
7.5 °C

Procedure

A mixture of 15.0 g (47.5 mmol) PRON-HCl, 170 mL MTBE and 20 mL water is cooled to 5 to 10° C. in a 250 mL vessel. After addition of 12.8 g of a 20% NaOH solution the mixture is stirred for further 15 min, while phase separation occurs. The organic phase is washed with water (60 mL) and the aqueous phase is extracted with MTBE (2×50 mL). The combined organic phases are cooled to below 10° C. and within 15 min a suspension of 8.6 g (45 mmol) p-toluenesulfonic acid monohydrate in 400 mL MTBE is added. An oily suspension is formed. The volume of the solvent is reduced to approximately the half. The reaction mixture is heated under reflux and 250 mL heptane are added. The mixture is cooled to RT and stirred for 30 min. The solid matter is filtered off, washed with MTBE (2×60 mL) and dried in vacuo at 50 to 55° C. affording 14.3 g of product (tan solid matter).

Workup

  1. washThe organic phase is washed with water (60 mL)
  2. extractionthe aqueous phase is extracted with MTBE (2×50 mL)
  3. temperatureThe combined organic phases are cooled to below 10° C. and within 15 min
  4. additionis added
  5. customAn oily suspension is formed
  6. temperatureThe reaction mixture is heated
  7. temperatureunder reflux
  8. temperatureThe mixture is cooled to RT
  9. stirringstirred for 30 min
  10. filtrationThe solid matter is filtered off
  11. washwashed with MTBE (2×60 mL)
  12. customdried in vacuo at 50 to 55° C.

Sources & evidence

ORD record
ord-4665a9a66b4b42da99ca8873fcfbe6bf
Source dataset
uspto-grants-2012_06
Patent number
US08193380B2

Reaction notes

Loading…