Ammonia → 2-Amino-6-nitrophenol

HRID 842093노트

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HRID 842093 반응식
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([N+:10]([O-])=O)[C:5]=1[OH:13])([O-:3])=[O:2].N.[Cl-].[NH4+].O.O.O.O.O.O.O.O.O.[S-2].[Na+].[Na+].Cl>O>[NH2:10][C:6]1[CH:7]=[CH:8][CH:9]=[C:4]([N+:1]([O-:3])=[O:2])[C:5]=1[OH:13]

참가 물질

7

반응물 5

HCID 222AmmoniaHCID 313Hydrochloric AcidHCID 113122,6-DinitrophenolHCID 25517Ammonium ChlorideHCID 73972Sodium sulfide nonahydrate

생성물 1

HCID 51272912-Amino-6-nitrophenol수율 68.3%

시약·촉매·용매 1

HCID 962Water용매2회

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온도
70 °C

실험 절차

A suspension of 2,6-dinitrophenol (5 g), ammonia (3 ml) and ammonium chloride (14.30 g) in water (30 ml) was heated to 70° C. A solution of sodium sulphide nonahydrate (24.19 g) in water (23 ml) was added and the resulting mixture stirred at 70° C. for 2 hours. The reaction was cooled to room temperature, acidified (pH 3.2) with 2N HCl, and the brown precipitate separated by filtration. The filtrate was extracted with chloroform (6×75 ml), the organic extracts combined with the precipitate, and evaporated in-vacuo to yield a dark brown solid. The solid was purified by flash chromatography (SiO2; dichloromethane) to yield the title compound (2.86 g, 68%) as a brown solid.

후처리

  1. temperatureThe reaction was cooled to room temperature
  2. customthe brown precipitate separated by filtration
  3. extractionThe filtrate was extracted with chloroform (6×75 ml)
  4. customevaporated in-vacuo
  5. customto yield a dark brown solid
  6. customThe solid was purified by flash chromatography (SiO2; dichloromethane)

출처 및 근거

ORD 기록
ord-95f6ea7ffb254dc899a0187a069e42c5
출처 데이터셋
uspto-grants-2002_04
특허 번호
US06372770B1

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