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Methanethiol → Methyl 2-methoxy-6-(methylthio)-nicotinate

HRID 372213
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HRID 372213 반응식
C[O-].[Na+].[CH3:4][SH:5].[CH3:6][O:7][C:8]1[N:17]=[C:16](Cl)[CH:15]=[CH:14][C:9]=1[C:10]([O:12][CH3:13])=[O:11]>CO>[CH3:6][O:7][C:8]1[N:17]=[C:16]([S:5][CH3:4])[CH:15]=[CH:14][C:9]=1[C:10]([O:12][CH3:13])=[O:11]
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참가 물질

5

반응물 3

HCID 878MethanethiolHCID 10560015Methyl 6-chloro-2-methoxynicotinateHCID 10942334Sodium Methoxide

생성물 1

HCID 20328808Methyl 2-methoxy-6-(methylthio)-nicotinate

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To 10 ml of a 1 N methanolic sodium methoxide solution are added dropwise 3 ml of a 3.5 N methanolic methylmercaptan solution. To the resultant methylmercaptide solution is added a solution of 2.01 g (0.01 mole) of methyl 2-methoxy-6-chloronicotinate (cf. Example 6 a)) in 30 ml of methanol. The reaction mixture is refluxed for 5 hours and the solvent is thereafter evaporated in vacuo. The residue is treated with 30 ml of saturated potassium carbonate solution and 150 ml of methylene chloride and separated in a separating funnel. The methylene chloride solution is dried over sodium sulphate and subsequently evaporated to dryness in vacuo. The crystallised residue is recrystallised from pentane and yields the methyl 2-methoxy-6-(methylthio)-nicotinate with a melting point of 71°-75° C.

후처리

  1. temperatureThe reaction mixture is refluxed for 5 hours
  2. customthe solvent is thereafter evaporated in vacuo
  3. additionThe residue is treated with 30 ml of saturated potassium carbonate solution and 150 ml of methylene chloride
  4. customseparated in a separating funnel
  5. dry with materialThe methylene chloride solution is dried over sodium sulphate
  6. customsubsequently evaporated to dryness in vacuo
  7. customThe crystallised residue is recrystallised from pentane

출처 및 근거

ORD 기록
ord-e14b28e3b0f841968c9aa89ac9d3dd52
출처 데이터셋
uspto-grants-1978_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04089960

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