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Methanol → Methyl 3-bromo-6-(phenylthio)-benzoate

HRID 435631
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반응식

HRID 435631 반응식
[Br:1][C:2]1[CH:3]=[C:4]([C:8]([S:11][C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[CH:9][CH:10]=1)[C:5]([OH:7])=[O:6].[CH3:18]O>S(=O)(=O)(O)O>[Br:1][C:2]1[CH:3]=[C:4]([C:8]([S:11][C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)=[CH:9][CH:10]=1)[C:5]([O:7][CH3:18])=[O:6]
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참가 물질

4

반응물 2

HCID 887MethanolHCID 214560473-Bromo-6-(phenylthio)-benzoic acid

생성물 1

HCID 21481147Methyl 3-bromo-6-(phenylthio)-benzoate

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

478 g of 3-bromo-6-(phenylthio)-benzoic acid in 1.5 litres of methanol and 200 ml of concentrated sulphuric acid are heated under reflux for 8 hours. The solution is concentrated under reduced pressure, treated with water and extracted with water. The organic solution is washed with aqueous sodium bicarbonate solution, dried over magnesium sulphate and concentrated under reduced pressure. There is obtained methyl 3-bromo-6-(phenylthio)-benzoate as a yellow oil.

후처리

  1. temperatureunder reflux for 8 hours
  2. concentrationThe solution is concentrated under reduced pressure
  3. additiontreated with water
  4. extractionextracted with water
  5. washThe organic solution is washed with aqueous sodium bicarbonate solution
  6. dry with materialdried over magnesium sulphate
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-ca0f3d8f232543b5b12f4da66edcf61d
출처 데이터셋
uspto-grants-1977_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04006145

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