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O[C:2]1([CH3:11])[CH:6]([CH2:7][C:8]#[CH:9])[C:5](=[O:10])[CH:4]=[CH:3]1.[OH-:12].[Na+].[Na+].[Cl-]>O>[CH2:7]([C:6]1[C:5](=[O:10])[CH2:4][CH:3]([OH:12])[C:2]=1[CH3:11])[C:8]#[CH:9]참가 물질
실험 절차
Into a reaction vessel, a solution of 4-hydroxy-4-methyl-5-propargyl-2-cyclopentenone (3 g) and MgCl2.6H2O (4.0 g) in water (120 ml) was charged, and the temperature was elevated up to 100° C. The contents were adjusted to pH 6.8 with 0.1 N NaOH solution, and stirring was continued at 100° C. for 4 hours, during which the pH was maintained at 6.8 to 7.0. After cooling, NaCl (40 g) was added to the reaction mixture and extracted with ether (120 ml) 4 times. The extracts were combined together, dried over anhydrous magnesium sulfate and concentrated at 40° C. under reduced pressure to give an oily substance (2.5 g). The oily substance was chromatographed with silica gel (30 g), followed by development with a solvent mixture of ethyl acetate and hexane (1:2 by volume) to give 2-propargyl-3-methyl-4-hydroxy-2-cyclopentenone (2.3 g). Yield, 77%. N.M.R. (CDCl3, internal standard TMS, δ ppm, 90 MHz): 4.60 (broad d, 1H, 4-H); 3.95 (broad s, 1H, 4-OH); 3.04 (d, 2H, --CH2 --C≡H); 2.65 (d of d, 1H, 5-H); 2.38 (d of d, 1H, 5 -H); 2.20 (s, 3H, 3-CH3); 1.98 (s, 1H, C≡CH).
후처리
- customwas elevated up to 100° C
- temperaturethe pH was maintained at 6.8 to 7.0
- temperatureAfter cooling
- extractionextracted with ether (120 ml) 4 times
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated at 40° C. under reduced pressure
- customto give an oily substance (2.5 g)
- customThe oily substance was chromatographed with silica gel (30 g)
- additionfollowed by development with a solvent mixture of ethyl acetate and hexane (1:2 by volume)
출처 및 근거
- ORD 기록
- ord-4249e371c04c4be6926d6fa3f075b1fe
- 출처 데이터셋
- uspto-grants-1982_08
- 특허 번호
- US04347386
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