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Boron tribromide → HCID 67606759、化合物

HRID 1626971
ノート
印刷プレビュー

反応式

HRID 1626971 の反応式
[Br:1][C:2]1[C:10]2[N:9]=[N:8][N:7]([CH2:11][CH:12]3[CH2:14][CH2:13]3)[C:6]=2[CH:5]=[CH:4][C:3]=1[O:15]C.B(Br)(Br)Br>ClCCl>[Br:1][C:2]1[C:10]2[N:9]=[N:8][N:7]([CH2:11][CH:12]3[CH2:14][CH2:13]3)[C:6]=2[CH:5]=[CH:4][C:3]=1[OH:15]
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

4

反応物 2

HCID 25134Boron tribromideHCID 67606434HCID 67606434、化合物

生成物 1

HCID 67606759HCID 67606759、化合物

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

4-Bromo-1-(cyclopropylmethyl)-5-methoxy-1H-benzotriazole (8.0 g, 28 mmol) was dissolved in dichloromethane (200 mL), cooled to 0° C. and treated with boron tribromide (57 mL, 1 M dichloromethane solution, 57 mmol, 2 equiv). The ice bath was removed and the mixture was warmed to ambient temperature and stirred for 4 hours. The mixture was treated slowly with water (exotherm), the pH of the solution was adjusted to pH>10 with 1 N aqueous sodium hydroxide and stirred for an additional 30 minutes. The pH of the mixture was then adjusted to pH 6-7 with ammonium chloride (aqueous saturated) and extracted exhaustively with dichloromethane containing 5% methanol. The combined organic extracts were dried with sodium sulfate, filtered and concentrated in vacuo, providing the titled compound.

後処理

  1. customThe ice bath was removed
  2. temperaturethe mixture was warmed to ambient temperature
  3. additionThe mixture was treated slowly with water (exotherm)
  4. stirringstirred for an additional 30 minutes
  5. extractionextracted exhaustively with dichloromethane containing 5% methanol
  6. dry with materialThe combined organic extracts were dried with sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-15103ac3bf4f46058bdff8e55ca32a26
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08785481B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート