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HCID 13592259、化合物 → 3,3-Bis(azidomethyl)oxetane

HRID 568994
ノート
印刷プレビュー

反応式

HRID 568994 の反応式
O[CH2:2][C:3]([CH2:12][O:13]S(C1C=CC(C)=CC=1)(=O)=O)([CH2:8][N:9]=[N+:10]=[N-:11])[CH2:4][N:5]=[N+:6]=[N-:7]>O1CCOCC1>[N:9]([CH2:8][C:3]1([CH2:4][N:5]=[N+:6]=[N-:7])[CH2:2][O:13][CH2:12]1)=[N+:10]=[N-:11]
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

3

反応物 1

HCID 13592259HCID 13592259、化合物

生成物 1

HCID 127253383,3-Bis(azidomethyl)oxetane

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

反応条件

温度
60 °C

実験手順

0.1 mole of compound 9 was dissolved in 100 ml of dry dioxane. 0.15 Mole of potassium tert.-butylate was added, with exclusion of moisture. After the reaction mixture had been stirred at 60° C. for 3 hours, it was concentrated. The residue was taken up in 400 ml of ether and the mixture was washed twice with 5% strength (weight: volume) aqueous NaCl solution. The organic phase was dried and concentrated in vacuo. The uniform product was further purified by column chromatography (eluting agent: chloroform/ethyl acetate 5:1).

後処理

  1. concentrationit was concentrated
  2. washthe mixture was washed twice with 5% strength (weight: volume) aqueous NaCl solution
  3. customThe organic phase was dried
  4. concentrationconcentrated in vacuo
  5. customThe uniform product was further purified by column chromatography (eluting agent: chloroform/ethyl acetate 5:1)

出典と根拠

ORDレコード
ord-07f45846d5b846cb9500043b92616995
出典データセット
uspto-grants-1988_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04730069

反応ノート

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