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Water → CGP-47292 methyl ester

HRID 541034
ノート
印刷プレビュー

反応式

HRID 541034 の反応式
[N:1]([CH2:4][C:5]1[C:10]([F:11])=[CH:9][CH:8]=[CH:7][C:6]=1[F:12])=[N+:2]=[N-:3].Br[C:14](=[CH2:19])[C:15]([O:17][CH3:18])=[O:16].O>C(O)(C)(C)C>[F:12][C:6]1[CH:7]=[CH:8][CH:9]=[C:10]([F:11])[C:5]=1[CH2:4][N:1]1[CH:19]=[C:14]([C:15]([O:17][CH3:18])=[O:16])[N:3]=[N:2]1
参加物反応条件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 962WaterHCID 229990Methyl 2-bromoacrylateHCID 108883232-(Azidomethyl)-1,3-difluorobenzene

生成物 1

HCID 22716778CGP-47292 methyl ester

試薬・触媒・溶媒 1

HCID 6386tert-Butanol溶媒

反応条件

温度
77.5 °C

実験手順

A mixture of 2-(azidomethyl)-1,3-difluorobenzene in t-butanol prepared as per example 2, methyl 2-bromoacrylate (120 gms) and water (200 ml) were heated to 75-80° C. The contents was stirred at 75-80° C. for 24 hours. After the completion of reaction, the reaction mixture was cooled to room temperature. The solid obtained was filtered and then crude mass was added to cyclohexane (240 ml) and the mixture was stirred at room temperature for 2 hours. The solid was filtered and washed with cyclohexane (50 ml). The product was dried for 2 hours to give methyl 1-(2,6-difluorobenzyl)-1H-1,2,3-triazole-4-carboxylate. Yield: 120 gms

後処理

  1. customAfter the completion of reaction
  2. temperaturethe reaction mixture was cooled to room temperature
  3. customThe solid obtained
  4. filtrationwas filtered
  5. additioncrude mass was added to cyclohexane (240 ml)
  6. stirringthe mixture was stirred at room temperature for 2 hours
  7. filtrationThe solid was filtered
  8. washwashed with cyclohexane (50 ml)
  9. customThe product was dried for 2 hours

出典と根拠

ORDレコード
ord-f9f4a9e1f2b049fba33409a8d9ac7437
出典データセット
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08871945B2

反応ノート

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