Potassium Hydroxide → HCID 15582646, compound

HRID 1868658Notes

Reaction equation

HRID 1868658 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:13])([CH2:11][CH3:12])[C:9]#N)=[CH:4][CH:3]=1.[OH-:14].[K+].CCO.[OH2:19]>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([CH3:13])([CH2:11][CH3:12])[C:9]([OH:19])=[O:14])=[CH:4][CH:3]=1

Participants

4

Conditions

Temperature
120 °C

Procedure

A mixture of 2-(4-chlorophenyl)-2-methylbutanenitrile-(6.5 g, 34 mmol) in 50 mL EtOH/H2O (5:1) was treated with KOH (3.8 g, 67 mmol). The mixture was stirred at 120° C. for 4 hours and then at 180° C. for 30 minutes. The mixture was cooled to room temperature. The mixture was extracted with EtOAc and the organic layer discarded. The water layer was acidified with concentrated HCl, extracted with EtOAc, washed with H2O and brine, dried over anhydrous Na2SO4, and concentrated in vacuo to give 1.16 g of the product as a pale yellow oil. MS m/e=213 (M+H)+.

Workup

  1. waitat 180° C. for 30 minutes
  2. temperatureThe mixture was cooled to room temperature
  3. extractionThe mixture was extracted with EtOAc
  4. extractionextracted with EtOAc
  5. washwashed with H2O and brine
  6. dry with materialdried over anhydrous Na2SO4
  7. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-bc035cbde48a4fe4bb0ce71dc66dbcb3
Source dataset
uspto-grants-2009_12
Patent number
US07635715B2

Reaction notes

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