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Water → HCID 18348181、化合物

HRID 2267967
ノート
印刷プレビュー

反応式

HRID 2267967 の反応式
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9]=[N:10][NH:11][N:12]=2)=[CH:4][CH:3]=1.C(=O)([O-])[O-].[K+].[K+].Br[CH2:20][CH2:21][F:22].O>C(#N)C>[F:22][CH2:21][CH2:20][N:11]1[N:12]=[C:8]([C:5]2[CH:4]=[CH:3][C:2]([CH3:1])=[CH:7][CH:6]=2)[N:9]=[N:10]1
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 CarbonateHCID 129822-Fluoroethyl bromideHCID 2851645-(4-Methylphenyl)-1H-tetrazole

生成物 1

HCID 18348181HCID 18348181、化合物収率 43.8%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

Under a nitrogen atmosphere, a stirred solution of 5.0 grams (0.031 mole) 4-(4-methylphenyl)-1,2,3,5-(1H)-tetrazole and 4.8 grams (0.035 mole) of potassium carbonate in 150 mL of acetonitrile was heated to reflux and then cooled to ambient temperature. To this was slowly added 10.0 grams (0.078 mole) of 1-bromo-2-fluoroethane. Upon completion of the addition the reaction mixture was placed in a water bath and cooled to 0° C., where it stirred for one hour. After this time the reaction mixture was heated to reflux, where it stirred for three hours, and then cooled to 0° C., where it stirred for about 18 hours. At the conclusion of this period the reaction mixture was poured into 50 mL of water. The resulting solution was extracted with three 50 mL portions of ethyl acetate. The combined extracts were concentrated under reduced pressure to a residue, which was subjected to column chromatography on silica gel. Elution was accomplished with methylene chloride and acetone. The product-containing fractions were combined and concentrated under reduced pressure, yielding 2.8 grams 1-(2-fluoroethyl)-(4-methylphenyl)-1,2,3,5-(1H)-tetrazole. The NMR spectrum was consistent with the proposed structure.

後処理

  1. temperatureto reflux
  2. additionUpon completion of the addition the reaction mixture
  3. customwas placed in a water bath
  4. temperaturecooled to 0° C.
  5. temperatureAfter this time the reaction mixture was heated
  6. temperatureto reflux
  7. stirringwhere it stirred for three hours
  8. temperaturecooled to 0° C.
  9. stirringwhere it stirred for about 18 hours
  10. extractionThe resulting solution was extracted with three 50 mL portions of ethyl acetate
  11. concentrationThe combined extracts were concentrated under reduced pressure to a residue, which
  12. washElution
  13. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-9ec13a3d4ad3458d996cabd1ea83c885
出典データセット
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
USH0002007H1

反応ノート

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