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Indene → 1-tert-Butyl-1H-indene

HRID 1279674
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HRID 1279674 반응식
[CH2:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1.[C:10](Br)([CH3:13])([CH3:12])[CH3:11]>[OH-].[K+]>[C:10]([CH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[CH:2]1)([CH3:13])([CH3:12])[CH3:11]
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참가 물질

4

반응물 2

HCID 7219IndeneHCID 10485t-Butyl bromide

생성물 1

HCID 5463021-tert-Butyl-1H-indene

시약·촉매·용매 1

HCID 14797Potassium Hydroxide용매

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온도
60 °C

실험 절차

42.0 g of indene (technical grade, 94 % by GC, 39.5 g, 340 mmol), 50 % w aqueous KOH (308 g in 308 nL) and 15.8 g of Adogen (Aldrich, 34 mnuol) dissolved in 139.7 g of tert-butylbromide (1019.6 mmol) were introduced in this order, at room temperature, in a 1 L, jacketed glass reactor with mechanical stirrer (Buïchi). The organic phase turns green. The mixture is heated to 60° C. and vigorously stirred for two hours (a pressure build-up to 2.5 bar-g is observed) and then cooled to room temperature. Total reaction time is 3 h. The organic phase is extracted with technical hexane (3×200mL) and analyzed by GC. Conversion: 74.5% w of 3-tert-butyl-indene and 1.8% of 1-tert-butyl-indene, unreacted indene 13.7% w. The solution was evaporated under reduced pressure (rotovac) and the resulting dark brown viscous liquid was distilled at 1 mmHg, collecting the fraction boiling between 70 and 80° C. (40 g, 76.8% of 3-tert-butyl-indene and 19.5% of 1-tert-butyl-indene, no indene).

후처리

  1. additionwere introduced in this order, at room temperature, in a 1 L
  2. temperaturethen cooled to room temperature
  3. waitTotal reaction time is 3 h
  4. extractionThe organic phase is extracted with technical hexane (3×200mL)
  5. customThe solution was evaporated under reduced pressure (rotovac)
  6. distillationthe resulting dark brown viscous liquid was distilled at 1 mmHg
  7. customcollecting the fraction
  8. customboiling between 70 and 80° C.

출처 및 근거

ORD 기록
ord-42ca32022f65478c86a86a809e77bfa1
출처 데이터셋
uspto-grants-2002_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06448350B1

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