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

HRID 648254ノート

反応式

HRID 648254 の反応式
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]

参加物

9

反応物 6

HCID 4764PhenolphthaleinHCID 112682-Bromoisovaleric acidHCID 11430Potassium CarbonateHCID 679842-Fluoro-4-methylanilineHCID 10942334Sodium MethoxideHCID 86719931NaOH ether

生成物 1

HCID 20482718alpha-(2-Fluoro-4-methylphenylamino)isovaleric acid

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 12679Hexamethylphosphoramide溶媒

実験手順

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.)

後処理

  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

出典と根拠

ORDレコード
ord-b00407b544244c2b81d8fcdf8b143daa
出典データセット
uspto-grants-1983_10
特許番号
US04411912

反応ノート

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