반응식
[OH-].[K+].[OH:3][CH2:4][C:5]1[O:6][CH:7]=[CH:8][C:9](=[O:12])[C:10]=1[OH:11].I[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20]>C(O)C.O>[OH:3][CH2:4][C:5]1[O:6][CH:7]=[CH:8][C:9](=[O:12])[C:10]=1[O:11][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20]참가 물질
실험 절차
To a solution of 2.75 g (0.042 mole) of potassium hydroxide in 38 ml of ethanol and 10 ml of water was added 5.93 g (0.042 mole) of 2-hydroxymethyl-3-hydroxy-4-pyrone, and the resulting mixture heated to 50°. A 12.4 g (0.046 mole) portion of ethyl 6-iodohexanoate was then added and the resulting clear solution heated at reflux for 7 hr under a nitrogen atomsphere. Removal of the ethanol under reduced pressure left a residue which was dissolved in methylene chloride. The organic solution was washed successively with aqueous NaHCO3 and saturated brine, was dried over magnesium sulfate, and was evaporated to afford a viscous oil. This material was chromatographed on silica gel eluting with ethyl acetate to give 6.34 g (54%) of oily product, 2-hydroxymethyl-3-(5-carboethoxypentyloxy)-4-pyrone: NMR (CDCl3): δ1.22 (3H, t, J = 7Hz), 2.30 (2H, t, J = 5.5 Hz), 4.63 (2H, s), 6.35 (1H, d, J = 6 Hz), 7.73 (1H, d, J = 6 Hz).
후처리
- temperaturethe resulting mixture heated to 50°
- temperaturethe resulting clear solution heated
- temperatureat reflux for 7 hr under a nitrogen atomsphere
- customRemoval of the ethanol under reduced pressure
- waitleft a residue which
- dissolutionwas dissolved in methylene chloride
- washThe organic solution was washed successively with aqueous NaHCO3 and saturated brine
- dry with materialwas dried over magnesium sulfate
- customwas evaporated
- customto afford a viscous oil
- customThis material was chromatographed on silica gel eluting with ethyl acetate
출처 및 근거
- ORD 기록
- ord-c5639ed8186d4c33b3e3c914a0c3f87e
- 출처 데이터셋
- uspto-grants-1979_01
- 특허 번호
- US04132847
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