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Ammonium Hydroxide → 2-Di-n-propylamino-8-(fur-3-yl)-1,2,3,4-tetrahydronaphthalene

HRID 22134
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HRID 22134 반응식
[CH2:1]([N:4]([CH2:16][CH2:17][CH3:18])[CH:5]1[CH2:14][CH2:13][C:12]2[C:7](=[C:8](Br)[CH:9]=[CH:10][CH:11]=2)[CH2:6]1)[CH2:2][CH3:3].[Mg].Br[C:21]1[CH:25]=[CH:24][O:23][CH:22]=1.[OH-].[NH4+]>C1COCC1.BrC(Br)C.C1(C)C=CC=CC=1.C1C=CC([P]([Ni]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.Cl[Ni](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.O>[CH2:1]([N:4]([CH2:16][CH2:17][CH3:18])[CH:5]1[CH2:14][CH2:13][C:12]2[C:7](=[C:8]([C:21]3[CH:25]=[CH:24][O:23][CH:22]=3)[CH:9]=[CH:10][CH:11]=2)[CH2:6]1)[CH2:2][CH3:3]
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참가 물질

11

반응물 4

HCID 14923Ammonium HydroxideHCID 891643-Bromofuran2회HCID 5462224MagnesiumHCID 145295648-Bromo-2-dipropylamino-1,2,3,4-tetrahydronaphthalene

생성물 1

HCID 152224292-Di-n-propylamino-8-(fur-3-yl)-1,2,3,4-tetrahydronaphthalene수율 84.1%

시약·촉매·용매 6

HCID 11201
1,1-Dibromoethane
촉매
HCID 178418751HCID 178418751, 화합물촉매
HCID 178420538HCID 178420538, 화합물촉매2회
HCID 962Water용매
HCID 1140Toluene용매
HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

2-Di-n-propylamino-8-bromo-1,2,3,4-tetrahydronaphthalene (1.0 g; 3.2 mmol) was dissolved in 20 ml of THF, and 94 mg (3.9 mmol) of magnesium shavings were added. The mixture was refluxed, and a couple of drops of dibromoethane were added to initiate Grignard formation. The mixture was refluxed for one hour after which it was added to a solution of 0.58 ml (6.4 mmol) of 3-bromofuran and 36 mg (0.03 mmol) of Ni(PPh3)4 in 20 ml of toluene that had been cooled to 0° C. after stirring at room temperature for one hour. The mixture was stirred at room temperature for three hours after which an additional 0.58 ml of 3-bromofuran and 35 mg of Ni(PPh3)4 were added. When the reaction failed to proceed further, 210 mg (0.3 mmol) Ni(PPh3)2Cl2 was added, and the mixture was stirred overnight at room temperature. The mixture then was poured into water and the pH adjusted to 10 with ammonium hydroxide. The mixture was extracted with methylene chloride, dried over sodium sulfate, and evaporated to give 0.8 g of a residue.

후처리

  1. temperatureThe mixture was refluxed
  2. temperatureThe mixture was refluxed for one hour after which it
  3. additionwere added
  4. stirringthe mixture was stirred overnight at room temperature
  5. extractionThe mixture was extracted with methylene chloride
  6. dry with materialdried over sodium sulfate
  7. customevaporated

출처 및 근거

ORD 기록
ord-d34262a676634d269babbf51150d3970
출처 데이터셋
uspto-grants-1995_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05426226

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