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Tetrahydrofuran → HCID 22929816、化合物

HRID 1295988
ノート
印刷プレビュー

反応式

HRID 1295988 の反応式
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[N:20]([CH2:23][C:24]1[C:25]([C:31]#[N:32])=[N:26][C:27]([CH3:30])=[CH:28][CH:29]=1)=[N+]=[N-].O1CCCC1>O>[CH3:30][C:27]1[N:26]=[C:25]2[C:31]([NH2:32])=[N:20][CH2:23][C:24]2=[CH:29][CH:28]=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 8028TetrahydrofuranHCID 11776TriphenylphosphineHCID 229298063-(Azidomethyl)-6-methyl-2-pyridinecarbonitrile

生成物 1

HCID 22929816HCID 22929816、化合物収率 34%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Triphenylphosphine (11 g, 42 mmol) was added to a mixed solution of 3-(azidomethyl)-6-methyl-2-pyridinecarbonitrile (5.79 g, 33.4 mmol) in a tetrahydrofuran (120 ml) —H2O (6 ml) mixed solvent while cooling on ice and the mixture was stirred at room temperature for 22 hours. The solvent was distilled off under reduced pressure and the residue was purified by silica gel column chromatography. The solvent was distilled off from the ethyl acetate-methanol-29% aqueous ammonia (40:10:1) elution fraction, and washing was performed with ether-n-hexane to yield the title compound (1.65 g, 34%) as a brown solid. The solvent was also distilled off from the washed mother liquor to yield the title compound (0.49 g). The NMR data for both compounds matched exactly.

後処理

  1. additionmixed solvent
  2. temperaturewhile cooling on ice
  3. distillationThe solvent was distilled off under reduced pressure
  4. customthe residue was purified by silica gel column chromatography
  5. distillationThe solvent was distilled off from the ethyl acetate-methanol-29% aqueous ammonia (40:10:1) elution fraction
  6. washwashing

出典と根拠

ORDレコード
ord-f92757abb08246bba41aea0ec66c9395
出典データセット
uspto-grants-2007_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07244730B2

反応ノート

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