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Sodium Hydroxide → 3-(4-Methoxybenzylmercapto)-4-n-butyl-1,2,4-triazole

HRID 1112108
ノート
印刷プレビュー

反応式

HRID 1112108 の反応式
[SH:1][C:2]1[N:6]([CH2:7][CH2:8][CH2:9][CH3:10])[CH:5]=[N:4][N:3]=1.[OH-].[Na+].[CH3:13][O:14][C:15]1[CH:22]=[CH:21][C:18]([CH2:19]Cl)=[CH:17][CH:16]=1>CO>[CH3:13][O:14][C:15]1[CH:22]=[CH:21][C:18]([CH2:19][S:1][C:2]2[N:6]([CH2:7][CH2:8][CH2:9][CH3:10])[CH:5]=[N:4][N:3]=2)=[CH:17][CH:16]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 14798Sodium HydroxideHCID 699934-Methyloxybenzyl chlorideHCID 178448642HCID 178448642、化合物

生成物 1

HCID 128884523-(4-Methoxybenzylmercapto)-4-n-butyl-1,2,4-triazole

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a mixture of 10 g. (0.064 mole) of 3-mercapto-4-n-butyl-1,2,4-triazole and 2.6 g. (0.064 mole) of sodium hydroxide in 200 ml. of methanol was added 9.9 g. (0.064 mole) of p-methoxybenzyl chloride. The reaction mixture was heated at reflux about 20 hours. The solvent was evaporated off, the residue washed with water, dried and distilled. There was obtained 17.8 g. of yellow liquid distilling at 190°-205° C. at 0.03 mm. Nuclear magnetic resonance and ultraviolet spectra indicated this to be approximately an equal mixture of 3-(4-methoxybenzylmercapto)-4-n-butyl-1,2,4-triazole and 4-n-butyl-2-(4-methoxybenzyl)-1,2,4-triazoline-3-thione.

後処理

  1. additionTo a mixture of 10 g
  2. temperatureThe reaction mixture was heated
  3. temperatureat reflux about 20 hours
  4. customThe solvent was evaporated off
  5. washthe residue washed with water
  6. customdried
  7. distillationdistilled
  8. customThere was obtained 17.8 g
  9. distillationof yellow liquid distilling at 190°-205° C. at 0.03 mm
  10. additionan equal mixture of 3-(4-methoxybenzylmercapto)-4-n-butyl-1,2,4-triazole and 4-n-butyl-2-(4-methoxybenzyl)-1,2,4-triazoline-3-thione

出典と根拠

ORDレコード
ord-ebbb97db9f5c4841bd5f21355d8c6d9e
出典データセット
uspto-grants-1978_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04120864

反応ノート

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