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Formaldehyde → N-(benzotriazol-1-ylmethyl)cyclopentanamine

HRID 1676514
ノート
印刷プレビュー

反応式

HRID 1676514 の反応式
[NH:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[N:2]1.[CH:10]1([NH2:15])[CH2:14][CH2:13][CH2:12][CH2:11]1.[CH2:16]=O>CCOCC>[N:1]1([CH2:16][NH:15][CH:10]2[CH2:14][CH2:13][CH2:12][CH2:11]2)[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[N:2]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 712FormaldehydeHCID 2906CyclopentylamineHCID 178418385HCID 178418385、化合物

生成物 1

HCID 5235843N-(benzotriazol-1-ylmethyl)cyclopentanamine収率 90.3%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

実験手順

To the mixture of 36 g (0.3 mole) of benzotriazole and 30 mL (0.3 mole) of cyclopentylamine in 1400 mL of ether was added dropwise 22 mL (0.3 mole) of 37% aqueous formaldehyde. The reaction mixture was stirred at room temperature overnight. The solution was dried over calcium chloride, filtered and concentrated under pressure. Hexane was added under ice-cooled bath and the resulting solid was collected by filtration and washed with hexane dried to give 58.6 g of benzotriazol-1-ylmethyl-cyclopentyl-amine as a white solid.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. dry with materialThe solution was dried over calcium chloride
  2. filtrationfiltered
  3. concentrationconcentrated under pressure
  4. additionHexane was added under ice-
  5. temperaturecooled bath
  6. filtrationthe resulting solid was collected by filtration
  7. washwashed with hexane
  8. customdried

出典と根拠

ORDレコード
ord-1b8d0c09900b4c8f9b7c46447f75fbdc
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08003785B2

反応ノート

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