Water → Methyl 3-amino-2-methyl-6-methylthiobenzoate

HRID 1534161

반응식

HRID 1534161 반응식
O.O.O.O.O.O.O.O.O.[S-2:10].[Na+].[Na+].O.[NH2:14][C:15]1[C:16]([CH3:28])=[C:17]([C:22](SC#N)=[CH:23][CH:24]=1)[C:18]([O:20][CH3:21])=O.[CH3:29]I>C(O)C>[NH2:14][C:15]1[C:16]([CH3:28])=[C:17]([C:22]([CH3:29])=[CH:23][CH:24]=1)[C:18]([O:20][CH3:21])=[S:10]

참가 물질

6

반응물 4

HCID 962WaterHCID 6328Methyl iodideHCID 73972Sodium sulfide nonahydrateHCID 14801188Methyl 3-amino-2-methyl-6-thiocyanatobenzoate

생성물 1

HCID 54391819Methyl 3-amino-2-methyl-6-methylthiobenzoate수율 104.1%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution comprising 39.5 g of sodium sulfide nonahydrate and 110 ml of water, a solution comprising 32.9 g of methyl 3-amino-2-methyl-6-thiocyanobenzoate and 300 ml of ethanol, was dropwise added. The mixture was stirred at room temperature for 1.5 hours, and then 24 g of methyl iodide was dropwise added thereto under cooling with ice. The mixture was stirred at room temperature for 2 hours and then concentrated under reduced pressure. A saturated sodium chloride aqueous solution was added thereto, and the mixture was extracted with chloroform. The chloroform layer was dried over anhydrous sodium sulfate, and then the solvent was distilled off to obtain 30.1 g of the desired product. Oily substance.

후처리

  1. additionwas dropwise added
  2. temperatureunder cooling with ice
  3. stirringThe mixture was stirred at room temperature for 2 hours
  4. concentrationconcentrated under reduced pressure
  5. additionA saturated sodium chloride aqueous solution was added
  6. extractionthe mixture was extracted with chloroform
  7. dry with materialThe chloroform layer was dried over anhydrous sodium sulfate
  8. distillationthe solvent was distilled off

출처 및 근거

ORD 기록
ord-01748d795d1d4c959bdd937a792b0762
출처 데이터셋
uspto-grants-1992_02
특허 번호
US05087724

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