2-Propanethiol → N-Acetyl-DL-phenylglycine

HRID 1414855

反応式

HRID 1414855 の反応式
[C:1]([NH:4][C:5]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)(SC)[C:6]([OH:8])=[O:7])(=[O:3])[CH3:2].C(S)(C)C.C(=O)([O-])[O-].[K+].[K+].CO.O>O>[C:1]([NH:4][CH:5]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[C:6]([OH:8])=[O:7])(=[O:3])[CH3:2]

参加物

6

反応物 4

HCID 63642-PropanethiolHCID 11430Potassium CarbonateHCID 21485357HCID 21485357、化合物HCID 22242641Methanol--water (1/1)

生成物 1

HCID 85935N-Acetyl-DL-phenylglycine収率 90%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

340 Milligrams of N-acetylamino-α-methylthiophenylacetic acid, 240 mg of isopropyl mercaptan, and 351 mg of potassium carbonate were added to 10 ml of a methanol-water mixture (9:1), and refluxed for 3 hours. Following a reduced pressure concentration of the reaction mixture to approximately 1 ml, 20 ml of water was added to the concentrate, which was then extracted with ethyl acetate. The organic phase was dried with Glauber's salt, and concentrated under reduced pressure. The residue was crystallized from an ether-n-hexane system, to provide 247 mg of α-acetylaminophenylacetic acid. The yield was 90%.

後処理

  1. temperaturerefluxed for 3 hours
  2. additionwas added to the concentrate, which
  3. extractionwas then extracted with ethyl acetate
  4. dry with materialThe organic phase was dried with Glauber's salt
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was crystallized from an ether-n-hexane system

出典と根拠

ORDレコード
ord-a16b058b1d63453f9222fce9b6bf70df
出典データセット
uspto-grants-1977_01
特許番号
US04002682

関連ノート

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