Phenolphthalein → alpha-(2-Fluoro-4-methylphenylamino)isovaleric acid

HRID 648254Notes

Reaction equation

HRID 648254 reaction equation
Br[CH:2]([CH:6]([CH3:8])[CH3:7])[C:3]([OH:5])=[O:4].C1C=C2C(OC(C3C=CC(O)=CC=3)(C3C=CC(O)=CC=3)C2=CC=1)=O.C[O-].[Na+].C(=O)([O-])[O-].[K+].[K+].[F:42][C:43]1[CH:49]=[C:48]([CH3:50])[CH:47]=[CH:46][C:44]=1[NH2:45].[OH-].[Na+].CCOCC>CO.CN(P(N(C)C)(N(C)C)=O)C>[F:42][C:43]1[CH:49]=[C:48]([CH3:50])[CH:47]=[CH:46][C:44]=1[NH:45][CH:2]([CH:6]([CH3:8])[CH3:7])[C:3]([OH:5])=[O:4]

Participants

9

Procedure

A solution of α-bromoisovaleric acid (8.17 mmole) in methanol is titrated to the phenophthalein end point using sodium methoxide. The solvent is removed by rotoevaporation and then there is added potassium carbonate (1.69 g), 2-fluoro-4-methylaniline (16.38 mmole) and 3 ml HMPT. The reaction is heated at 60° for about 5 hours and then worked up with 5% sodium hydroxide/ether and washed with water (3×). The basic layer is acidified and extracted with ether, washed with water and brine, dried over sodium sulfate and rotoevaporated to yield α-(2-fluoro-4-methylphenylamino)isovaleric acid. (2-Fluoro-4-methylaniline is prepared from 3-fluoro-4-nitrotoluene in a Parr bottle using platinum oxide and hydrogen in ethanol.)

Workup

  1. customThe solvent is removed by rotoevaporation
  2. temperatureThe reaction is heated at 60° for about 5 hours
  3. washwashed with water (3×)
  4. extractionextracted with ether
  5. washwashed with water and brine
  6. dry with materialdried over sodium sulfate

Sources & evidence

ORD record
ord-b00407b544244c2b81d8fcdf8b143daa
Source dataset
uspto-grants-1983_10
Patent number
US04411912

Reaction notes

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