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Formaldehyde → N-Cyclobutyl-1H-benzotriazole-1-methanamine

HRID 1676501
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HRID 1676501 반응식
[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]C1.[CH2:16]=O>CCOCC>[N:1]1([CH2:16][NH:15][CH:10]2[CH2:12][CH2:13][CH2:14]2)[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[N:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 712FormaldehydeHCID 2906CyclopentylamineHCID 178418385HCID 178418385, 화합물

생성물 1

HCID 86637494N-Cyclobutyl-1H-benzotriazole-1-methanamine

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

To a mixture of 28.6 g (0.24 mole) benzotriazole and 17.6 g (0.24 mole) of cyclopentylamine in 1000 mL of ether was added dropwise, 19.5 mL (0.24 mole) of 37% aqueous formaldehyde. The reaction mixture was stirred at room temperature under for 18 hours. The mixture was dried over calcium chloride, filtered and concentrated under reduced pressure. Hexanes was added to the residue, concentrated under reduced pressure to give the crude benzotriazol-1-ylmethyl-cyclobutyl-amine as an oil, which was used in the next without further purification.

후처리

  1. additionwas added dropwise
  2. dry with materialThe mixture was dried over calcium chloride
  3. filtrationfiltered
  4. concentrationconcentrated under reduced pressure
  5. additionHexanes was added to the residue
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-6c9233427cba49e189cce271d793703e
출처 데이터셋
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08003785B2

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