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Water → 2-Difluoromethoxy-6-propylsulfanylbenzonitrile

HRID 229931
ノート
印刷プレビュー

反応式

HRID 229931 の反応式
[OH:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([S:10][CH2:11][CH2:12][CH3:13])[C:3]=1[C:4]#[N:5].C(=O)([O-])[O-].[K+].[K+].Br[CH:21]([F:23])[F:22].O>CN(C)C=O>[F:22][CH:21]([F:23])[O:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([S:10][CH2:11][CH2:12][CH3:13])[C:3]=1[C:4]#[N:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 11430Potassium Carbonate2 回HCID 62407Bromodifluoromethane2 回HCID 685669922-Hydroxy-6-propylsulfanylbenzonitrile

生成物 1

HCID 685651162-Difluoromethoxy-6-propylsulfanylbenzonitrile

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide
溶媒

実験手順

10.8 g (56 mmol) of 2-hydroxy-6-propylsulfanylbenzonitrile were dissolved in 120 ml of dimethylformamide, and 15.5 g (0.11 mol) of anhydrous potassium carbonate were added. Then, at room temperature, 8.2 g of bromodifluoromethane were passed in, and the mixture was stirred at room temperature for 5 hours. Then 15.5 g (0.11 mol) of anhydrous potassium carbonate and 7.2 g of bromodifluoromethane were added, and the mixture was stirred at room temperature overnight. The reaction mixture was worked up by pouring into water and extracting twice with methyl tert.-butyl ether. The organic phase was separated, washed several times with water and concentrated. The solid has been dried in vacuo at 50° C. Yield: 12.3 g of an oily residue.

後処理

  1. customat room temperature
  2. stirringthe mixture was stirred at room temperature overnight
  3. extractionextracting twice with methyl tert.-butyl ether
  4. customThe organic phase was separated
  5. washwashed several times with water
  6. concentrationconcentrated
  7. customThe solid has been dried in vacuo at 50° C

出典と根拠

ORDレコード
ord-8e25aa662d4b4dae9d49c8245bd9d31e
出典データセット
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07563921B2

反応ノート

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