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Ammonium Chloride → 3-benzyloxy-1-methyl-1H-pyrazol-4-ylacetonitrile

HRID 1295222
ノート
印刷プレビュー

反応式

HRID 1295222 の反応式
CC(C)([O-])C.[K+].C1(C)C=CC(S([CH2:16][N+:17]#[C-])(=O)=O)=CC=1.[CH2:20]([O:27][C:28]1[C:32]([CH:33]=O)=[CH:31][N:30]([CH3:35])[N:29]=1)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.[Cl-].[NH4+]>C(COC)OC.CO>[CH2:20]([O:27][C:28]1[C:32]([CH2:33][C:16]#[N:17])=[CH:31][N:30]([CH3:35])[N:29]=1)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=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

7

反応物 4

HCID 25517Ammonium ChlorideHCID 161915Tosylmethyl isocyanideHCID 229307233-(benzyloxy)-1-methyl-1H-pyrazole-4-carbaldehydeHCID 23665647Potassium tert-butoxide

生成物 1

HCID 694287193-benzyloxy-1-methyl-1H-pyrazol-4-ylacetonitrile収率 82%

試薬・触媒・溶媒 2

HCID 887
Methanol
溶媒
HCID 80711,2-Dimethoxyethane溶媒3 回

反応条件

温度
-78 °C

実験手順

To a mixture of potassium t-butoxide (2.24 g) and dimethoxyethane (10 ml) was added a solution of p-toluenesulfonylmethyl isocyanide (2.05 g) in dimethoxyethane (10 ml) and the mixture was stirred at −78° C. for 5 min. Then a solution of 3-benzyloxy-1-methyl-1H-pyrazole-4-carbaldehyde (2.16 g) in dimethoxyethane (10 ml) was added. After stirring at said temperature for 1 hr, the mixture was stirred for 1 hr. while raising the temperature to room temperature. To the obtained mixture was added methanol (380 ml), and the mixture was refluxed for 1 hr. After cooling, the reaction solution was poured into saturated aqueous ammonium chloride solution and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography, and 3-benzyloxy-1-methyl-1H-pyrazol-4-ylacetonitrile (1.86 g, yield 82%) was obtained as a colorless oil from a fraction eluted with ethyl acetate-hexane (1:2, volume ratio).

後処理

  1. stirringAfter stirring
  2. customfor 1 hr
  3. stirringthe mixture was stirred for 1 hr
  4. temperaturewhile raising the temperature to room temperature
  5. temperaturethe mixture was refluxed for 1 hr
  6. temperatureAfter cooling
  7. extractionthe mixture was extracted with ethyl acetate
  8. washThe ethyl acetate layer was washed with saturated brine
  9. dry with materialdried (MgSO4)
  10. concentrationconcentrated

出典と根拠

ORDレコード
ord-eff547795e414cdd9b7878b9e4443ea7
出典データセット
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07241785B2

反応ノート

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