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Hydrochloric Acid → 3-(4-Methylphenyl)-6-methylthiotetrahydro-1,3,5-triazine-2,4-dione

HRID 126764
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HRID 126764 반응식
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]=[C:9]=[O:10])=[CH:4][CH:3]=1.[NH2:11][C:12](=[N:15][C:16](=O)[O:17]C)[S:13][CH3:14].C[O-].[Na+].Cl>C(Cl)Cl>[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[C:16](=[O:17])[NH:15][CH:12]([S:13][CH3:14])[NH:11][C:9]2=[O:10])=[CH:4][CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 693254-Methylphenyl isocyanateHCID 2935781-methoxycarbonyl-S-methylisothioureaHCID 10942334Sodium Methoxide

생성물 1

HCID 538772003-(4-Methylphenyl)-6-methylthiotetrahydro-1,3,5-triazine-2,4-dione수율 81%

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매

실험 절차

4-Methylphenylisocyanate (19.0 g.) was added during 10 minutes to a solution of methyl N-[1-amino-1-(methylthio)methylene]carbamate (21.2 g.) in methylene chloride (200 ml.). After 2 hours of stirring, sodium methoxide [obtained by dissolving sodium (3.5 g.) in methanol (30 ml.)] was added at 15°-20° C. The subsequent mixture was stirred at that temperature for 18 hours and the resultant solid collected by filtration and dissolved in water (200 ml.). The solution obtained was acidified with concentrated hydrochloric acid and the solid which formed was collected by filtration, washed well with water and dried to give 3-(4-methylphenyl)-6-methylthiotetrahydro-1,3,5-triazine-2,4-dione (29 g., 81%), m.p. 276°-278° C.

후처리

  1. stirringThe subsequent mixture was stirred at that temperature for 18 hours
  2. filtrationthe resultant solid collected by filtration
  3. dissolutiondissolved in water (200 ml.)
  4. customThe solution obtained
  5. customthe solid which formed
  6. filtrationwas collected by filtration
  7. washwashed well with water
  8. customdried

출처 및 근거

ORD 기록
ord-08bda83688d34e06852d475c07644bc7
출처 데이터셋
uspto-grants-1981_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04254122

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