Potassium Hydroxide → Potassium alpha-isopropyl-4-chlorophenylacetate

HRID 894336Notes

Reaction equation

HRID 894336 reaction equation
[CH:1]([CH:4]([C:8]1[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][CH:9]=1)[C:5]([OH:7])=[O:6])([CH3:3])[CH3:2].[OH-].[K+:16]>C(O)C.O>[CH:1]([CH:4]([C:8]1[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][CH:9]=1)[C:5]([O-:7])=[O:6])([CH3:3])[CH3:2].[K+:16]

Participants

5

Reactant 2

HCID 14797Potassium HydroxideHCID 16197Benzeneacetic acid, 4-chloro-alpha-(1-methylethyl)-

Product 1

HCID 23685460Potassium alpha-isopropyl-4-chlorophenylacetate

Reagents, catalysts & solvents 2

HCID 702EthanolSolventHCID 962WaterSolvent

Procedure

α-Isopropyl-4-chlorophenylacetic acid (1.3 g) was dissolved in ethanol (10 ml) and a solution of potassium hydroxide (0.34 g) in water (5 ml) was added to the ethanolic solution. The solvents were then removed by distillation under reduced pressure to give anhydrous potassium α-isopropyl-4-chlorophenylacetate.

Workup

  1. customThe solvents were then removed by distillation under reduced pressure

Sources & evidence

ORD record
ord-087120f1d8154163b5d8e1a40fed35df
Source dataset
uspto-grants-1981_08
Patent number
US04283414

Reaction notes

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