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Hydrochloric Acid → 1-(3-Bromophenyl)ethanamine

HRID 1255832
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HRID 1255832 반응식
[Br:1][C:2]1[CH:3]=[C:4]([C:8](=O)[CH3:9])[CH:5]=[CH:6][CH:7]=1.C([O-])=O.[NH4+:14].Cl>CO.O.C[C]1[C](C)[C](C)[C](C)[C]1C.C[C]1[C](C)[C](C)[C](C)[C]1C.Cl[Rh]Cl.Cl[Rh]Cl>[Br:1][C:2]1[CH:3]=[C:4]([CH:8]([NH2:14])[CH3:9])[CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 313Hydrochloric AcidHCID 165023'-BromoacetophenoneHCID 2723923Ammonium formate

생성물 1

HCID 167857641-(3-Bromophenyl)ethanamine수율 85%

시약·촉매·용매 3

HCID 16212157Bis[(pentamethylcyclopentadienyl)dichloro-rhodium]촉매HCID 887
Methanol
용매
HCID 962Water용매

실험 절차

A mixture of 3′-bromoacetophenone (2.66 mL, 20 mmol), ammonium formate (6.31 g, 100 mmol) and dichloro(pentamethylcyclopentadienyl)rhodium(III) dimer (124 mg, 0.2 mmol) in anhydrous methanol (20 mL) under an atmosphere of nitrogen was heated at reflux for 5 hours then allowed to cool to room temperature overnight. The mixture was diluted with water (20 mL), acidified to pH 2 with dilute aqueous hydrochloric acid (2M) and washed with dichloromethane (2×60 mL). The aqueous solution was basified to pH 12 with solid potassium hydroxide, extracted with dichloromethane (3×50 mL) and the extracts washed with brine (50 mL), dried (Na2SO4) and concentrated under reduced pressure to give 1-(3-bromophenyl)ethanamine (3.4 mg, 85%) as a yellow liquid.

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 5 hours
  3. washwashed with dichloromethane (2×60 mL)
  4. extractionextracted with dichloromethane (3×50 mL)
  5. washthe extracts washed with brine (50 mL)
  6. dry with materialdried (Na2SO4)
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-0f2c8b8abbd44aa49c644c9fcf7dadab
출처 데이터셋
uspto-grants-2013_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08461161B2

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