Hydrochloric Acid → 2,2'-Diamino-4,4'-dibromobiphenyl

HRID 1821061

반응식

HRID 1821061 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([Br:14])=[CH:10][C:9]=2[N+:15]([O-])=O)=[C:4]([N+:18]([O-])=O)[CH:3]=1.Cl.[Sn].[OH-].[Na+]>C(O)C>[Br:1][C:2]1[CH:3]=[C:4]([NH2:18])[C:5]([C:8]2[C:9]([NH2:15])=[CH:10][C:11]([Br:14])=[CH:12][CH:13]=2)=[CH:6][CH:7]=1

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 5352426Tin atomHCID 100466484,4'-Dibromo-2,2'-dinitro-1,1'-biphenyl

생성물 1

HCID 112215382,2'-Diamino-4,4'-dibromobiphenyl

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
100 °C

실험 절차

To a solution of 15 (11.0 g, 27.4 mmol) in 135 mL of absolute ethanol was added 32% w/w aqueous HCl (78.0 mL). Tin powder (13.0 g, 108.5 mmol) was then added in portions over 10 min, and the reaction mixture was heated to reflux at 100° C. for 2 h. After cooling, the mixture was poured into ice water (400 mL) and then made alkaline with 20% w/w aqueous NaOH solution until the pH was 9.0. The product was next extracted with diethyl ether and the organic layer was washed with brine, dried over anhydrous Na2SO4, filtered, and then evaporated to dryness to give pure product as light-brown crystals that could be used without further purification (8.6 g, 92%). 1H NMR (CDCl3): δ 6.92 (6H, s), 3.78 (4H, br s, NH2) ppm; 13C NMR (CDCl3): δ 118.2, 121.9, 122.1, 122.8, 132.4, 145.3 ppm; m.p. 118-119° C.

후처리

  1. temperaturethe reaction mixture was heated
  2. temperatureAfter cooling
  3. extractionThe product was next extracted with diethyl ether
  4. washthe organic layer was washed with brine
  5. dry with materialdried over anhydrous Na2SO4
  6. filtrationfiltered
  7. customevaporated to dryness
  8. customto give pure product as light-brown crystals that
  9. customcould be used without further purification (8.6 g, 92%)

출처 및 근거

ORD 기록
ord-d7aac1d2f4264d34a8f1582882a5f98e
출처 데이터셋
uspto-grants-2009_10
특허 번호
US07605225B2

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