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Hydrochloric Acid → 3-Amino-5-bromobenzonitrile

HRID 1527460
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반응식

HRID 1527460 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([N+:10]([O-])=O)[CH:9]=1)[C:5]#[N:6].[Sn].Cl>CO>[NH2:10][C:8]1[CH:7]=[C:4]([CH:3]=[C:2]([Br:1])[CH:9]=1)[C:5]#[N:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 51524253-Bromo-5-nitrobenzonitrileHCID 5352426Tin atom

생성물 1

HCID 534069613-Amino-5-bromobenzonitrile

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of 3-bromo-5-nitrobenzonitrile (1 g, 4.4 mmol) in MeOH (50 mL) was added tin (5.23 g, 44 mmol) and 3N HCl (44 mL, 132 mmol). The reaction mixture was stirred at RT for 2 h, the filtered off and washed with MeOH. The filtrate was concentrated in vacuo, and the remaining water phase was basified to pH=12 by addition of 4N NaOH. The aqueous layer was extracted twice with EtOAc (100 mL), the combined organics were dried (Na2SO4) and evaporated in vacuo to afford the title compound as a yellowish solid. MS (LC/MS): 197.0 [M+H]+; tR (HPLC conditions c): 4.30 min.

후처리

  1. filtrationthe filtered off
  2. washwashed with MeOH
  3. concentrationThe filtrate was concentrated in vacuo
  4. additionthe remaining water phase was basified to pH=12 by addition of 4N NaOH
  5. extractionThe aqueous layer was extracted twice with EtOAc (100 mL)
  6. dry with materialthe combined organics were dried (Na2SO4)
  7. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-1c457af25d144eb8ad2304df9d8284ed
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09085555B2

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