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Phosphoric Acid → 1,3-Benzenediol, 4-methyl-

HRID 55713
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HRID 55713 반응식
[OH:1][C:2]1[CH:9]=[C:8]([OH:10])[CH:7]=[CH:6][C:3]=1[CH:4]=O.P(=O)(O)(O)O>CC(O)C.[Pd]>[CH3:4][C:3]1[CH:6]=[CH:7][C:8]([OH:10])=[CH:9][C:2]=1[OH:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 1004Phosphoric AcidHCID 72132,4-Dihydroxybenzaldehyde

생성물 1

HCID 103331,3-Benzenediol, 4-methyl-수율 98.1%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 3776Isopropanol용매

실험 절차

2,4-Dihydroxybenzaldehyde (33.97 gm, 0.246 mol) (recrystallized from toluene) was dissolved in spectroscopic grade 2-propanol (3 L) in a round bottom flask fitted with a gas inlet and a bubbler outlet. 10% Palladium on carbon (1.35 gm) was added followed by phosphoric acid (3 mL) and the mixture was sparged with nitrogen. The nitrogen flow was switched to hydrogen and the mixture was rapidly stirred with ice cooling. After 3 hours hydrogen uptake was complete and the catalyst was removed by filtration. The filtrate was stripped down to 200 mL and 200 mL of ethyl acetate was added. The solution was washed with 4×200 mL of water and the combined water extracts back-extracted with ethyl acetate. These organic extracts were water washed and the combined organic layers dried over sodium sulfate and striped down to afford the product as a colorless crystalline solid (29.95 gm, 98%). M.p.: 106° C. (Lit. 106°-107° C. [J. C. Bell, W. Bridge, and A. Robertson, J. Chem. Soc., 1542-45 (1937)]).

후처리

  1. customfitted with a gas inlet and a bubbler outlet
  2. customthe mixture was sparged with nitrogen
  3. customthe catalyst was removed by filtration
  4. additionwas added
  5. washThe solution was washed with 4×200 mL of water
  6. extractionthe combined water extracts back-extracted with ethyl acetate
  7. washwashed
  8. dry with materialthe combined organic layers dried over sodium sulfate

출처 및 근거

ORD 기록
ord-828bdc66e947456a81985c2b2a4c16c9
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05625081

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