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Urea → 2-Bromo-4-chlorobenzonitrile

HRID 251852
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반응식

HRID 251852 반응식
[Br:1][C:2]1[CH:10]=[C:9]([Cl:11])[CH:8]=[CH:7][C:3]=1[C:4](O)=O.[NH2:12]C(N)=O>ClCCl>[Br:1][C:2]1[CH:10]=[C:9]([Cl:11])[CH:8]=[CH:7][C:3]=1[C:4]#[N:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1176UreaHCID 331262-Bromo-4-chlorobenzoic acid

생성물 1

HCID 234985242-Bromo-4-chlorobenzonitrile

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

588 mg of 2-bromo-4-chlorobenzoic acid and 300 mg of urea are dissolved in dichloromethane/methanole and deposited onto 364 mg of aluminum oxide on a rotary evaporator. The residue is irradiated for 60 min in a microwave at 150° C. After cooling the residue is stirred with ethyl acetate and water, the mixture is filtered and the aqueous phase is removed. The organic phase is washed with a sodium hydrogencarbonate solution dried over sodium sulfate, concentrated on a rotary evaporator and then dried under high vacuum. The product is reacted further without additional purification.

후처리

  1. customdeposited onto 364 mg of aluminum oxide on a rotary evaporator
  2. customThe residue is irradiated for 60 min in a microwave at 150° C
  3. temperatureAfter cooling the residue
  4. filtrationthe mixture is filtered
  5. customthe aqueous phase is removed
  6. washThe organic phase is washed with a sodium hydrogencarbonate solution
  7. dry with materialdried over sodium sulfate
  8. concentrationconcentrated on a rotary evaporator
  9. customdried under high vacuum
  10. customThe product is reacted further without additional purification

출처 및 근거

ORD 기록
ord-76ae201f062f4fa79013a64f98874d37
출처 데이터셋
uspto-grants-2011_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07867992B2

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