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Trimethylhydroquinone → 6-Hydroxy-4,4,5,7,8-pentamethyl-3,4-dihydrocoumarin

HRID 921504
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HRID 921504 반응식
[CH3:1][C:2]1[C:8]([CH3:9])=[C:7]([OH:10])[C:6]([CH3:11])=[CH:5][C:3]=1[OH:4]>CS(O)(=O)=O>[OH:10][C:7]1[C:6]([CH3:11])=[C:5]2[C:3](=[C:2]([CH3:1])[C:8]=1[CH3:9])[O:4][C:3](=[O:4])[CH2:2][C:8]2([CH3:9])[CH3:7]
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참가 물질

3

반응물 1

HCID 12785Trimethylhydroquinone

생성물 1

HCID 6163496-Hydroxy-4,4,5,7,8-pentamethyl-3,4-dihydrocoumarin수율 75%

시약·촉매·용매 1

HCID 6395Methanesulfonic Acid용매

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온도
70 °C

실험 절차

A mixture of 2,3,5-trimethyl hydroquinone (10 g, 0.0657 mol) and methyl 1,1-dimethylacrylate (7.5 g, 0.0657) in 50 ml of methanesulfonic acid was heated to 70° C. for 2 hours. Upon cooling to room temperature, the mixture was poured into 100 ml of ice-cold water. The resulting mixture was extracted three times with ethyl acetate, and the combined organic layers were washed with water and dried over sodium sulfate. After removal of the majority of ethyl acetate, the mixture was cooled −20° C. The pale white solid was collected by filtration, washed with cold ethyl acetate and dried under vacuum oven. The yield was 75%. 1H NMR (300 MHz, CD2Cl2) δ ppm: 4.69 (s, 1H, OH), 2.59 (s, 2H, CH2), 2.53 (s, 3H, CH3), 2.35 (s, 3H, CH3), 2.20 (s, 3H, CH3), 1.57 (s, 3H, CH3), 1.44 (s, 3H, CH3); MS (m/e): 235 (M+).

후처리

  1. temperatureUpon cooling to room temperature
  2. extractionThe resulting mixture was extracted three times with ethyl acetate
  3. washthe combined organic layers were washed with water
  4. dry with materialdried over sodium sulfate
  5. customAfter removal of the majority of ethyl acetate
  6. temperaturethe mixture was cooled −20° C
  7. filtrationThe pale white solid was collected by filtration
  8. washwashed with cold ethyl acetate
  9. customdried under vacuum oven

출처 및 근거

ORD 기록
ord-c366c39f455b4474ba0797357a888149
출처 데이터셋
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09273343B2

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