Pyridine → 4-Hydroxycyclopent-2-en-1-yl acetate

HRID 2163160

반응식

HRID 2163160 반응식
[OH:1][CH:2]1[CH2:6][CH:5]([OH:7])[CH:4]=[CH:3]1.N1C=CC=CC=1.[C:14](Cl)(=[O:16])[CH3:15]>O1CCCC1>[C:14]([O:1][CH:2]1[CH2:6][CH:5]([OH:7])[CH:4]=[CH:3]1)(=[O:16])[CH3:15]

참가 물질

5

실험 절차

0.70 gram (7.0 mmols) of 3,5-dihydroxycyclopent-1-ene and 0.83 gram (10.5 mmols) of pyridine were dissolved in 20 milliliters of anhydrous tetrahydrofuran, after which a solution of 0.70 g (9.0 mmols) of acetic acid chloride in 6 milliliters of anhydrous tetrahydrofuran was added dropwise over a period of 15 hours at room temperature in a stream of dried nitrogen, using a syringe drive. After concentrating the solvent with a rotary evaporator, 20 milliliters of ethyl acetate was added, following which the reaction mixture was washed with dilute hydrochloric acid (5 ml × 2), saturated sodium bicarbonate solution (5 ml × 2) and saturated sodium chloride solution (5 ml × 2). The organic layer was then separated and dried with anhydrous sodium sulfate. On distilling off the solvent, 1.00 gram of a colorless oil substance was obtained.

후처리

  1. concentrationAfter concentrating the solvent
  2. customwith a rotary evaporator, 20 milliliters of ethyl acetate
  3. additionwas added
  4. washwas washed with dilute hydrochloric acid (5 ml × 2), saturated sodium bicarbonate solution (5 ml × 2) and saturated sodium chloride solution (5 ml × 2)
  5. customThe organic layer was then separated
  6. dry with materialdried with anhydrous sodium sulfate
  7. distillationOn distilling off the solvent

출처 및 근거

ORD 기록
ord-463818ef6a1e481f90874f8911e072da
출처 데이터셋
uspto-grants-1979_01
특허 번호
US04132726

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