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

HRID 1676502
ノート
印刷プレビュー

反応式

HRID 1676502 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) 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 to the residue cooled in an ice bath and the resulting solid was collected by filtration washing with hexane and then dried to give 58.6 g of benzotriazol-1-ylmethyl-cyclopentylamine 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 to the residue
  5. temperaturecooled in an ice bath
  6. filtrationthe resulting solid was collected by filtration
  7. washwashing with hexane
  8. customdried

出典と根拠

ORDレコード
ord-8e7777087605449c99f17a24f4b4211e
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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