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Bromomethyl 4-methoxyphenyl ketone → 3-(p-Methoxy-phenacylmercapto)-4-n-butyl-1,2,4-triazole

HRID 1112110
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반응식

HRID 1112110 반응식
[SH:1][C:2]1[N:6]([CH2:7][CH2:8][CH2:9][CH3:10])[CH:5]=[N:4][N:3]=1.[OH-].[Na+].Br[CH2:14][C:15]([C:17]1[CH:22]=[CH:21][C:20]([O:23][CH3:24])=[CH:19][CH:18]=1)=[O:16]>CO>[CH3:24][O:23][C:20]1[CH:21]=[CH:22][C:17]([C:15](=[O:16])[CH2:14][S:1][C:2]2[N:6]([CH2:7][CH2:8][CH2:9][CH3:10])[CH:5]=[N:4][N:3]=2)=[CH:18][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 4965Bromomethyl 4-methoxyphenyl ketoneHCID 14798Sodium HydroxideHCID 178448642HCID 178448642, 화합물

생성물 1

HCID 128884643-(p-Methoxy-phenacylmercapto)-4-n-butyl-1,2,4-triazole

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 3-mercapto-4-n-butyl-1,2,4-triazole (10 g. or 0.063 mole) and sodium hydroxide (2.55 g. or 0.0637 mole) in 200 ml. of methanol was added α-bromo-p-methoxyacetophenone (15.3 g. or 0.067 mole). The reaction mixture was heated at reflux for 16 hours and the solvent removed in vacuum to leave a solid residue. The solid was washed with water and recrystallized from benzene-hexane to give 3-(p-methoxy-phenacylmercapto)-4-n-butyl-1,2,4-triazole melting at 79°-82° C. The structure was confirmed by its infrared and nuclear magnetic spectra.

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux for 16 hours
  3. customthe solvent removed in vacuum
  4. customto leave a solid residue
  5. washThe solid was washed with water
  6. customrecrystallized from benzene-hexane

출처 및 근거

ORD 기록
ord-e9809cf5a2f34f45aba3e25b02b33eb1
출처 데이터셋
uspto-grants-1978_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04120864

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