Diethyl Ether → HCID 14838645, 화합물

HRID 1681856노트

반응식

HRID 1681856 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:13][CH:14]=C)[C:5]([OH:12])=[C:6]([CH:11]=1)[C:7]([O:9][CH3:10])=[O:8].CC[O:18]CC.I([O-])(=O)(=O)=O.[Na+]>[Os](=O)(=O)(=O)=O.O>[C:7]([C:6]1[C:5]([OH:12])=[C:4]([CH2:13][CH:14]=[O:18])[CH:3]=[C:2]([Cl:1])[CH:11]=1)([O:9][CH3:10])=[O:8]

참가 물질

6

반응물 3

HCID 3283Diethyl EtherHCID 14838644HCID 14838644, 화합물HCID 23667635Sodium periodate

생성물 1

HCID 14838645HCID 14838645, 화합물

시약·촉매·용매 2

HCID 30318Osmium Tetroxide촉매HCID 962Water용매2회

실험 절차

Osmium tetroxide (1.0 g, 3.9 mmol) was added to a mixture of methyl 5-chloro-2-hydroxy-3-(2-propenyl)benzoate (4c) (22.7 g, 0.1 mol), ether (400 ml), and water (400 ml). After stirring at room temperature for 5 minutes, sodium periodate (47.06 g, 0.22 mol) was added in portions. The mixture was stirred at room temperature for another 21 hours, and then poured into 800 ml of water. The layers were separated and the aqueous layer extracted with ethyl ether (2×400 ml). The organic layers were combined, dried over anhydrous Na2SO4 and then filtered through a column of Florisil (85 g) to remove inorganic impurity. Evaporation of the ether yielded 5c quantitatively as a brown solid, m.p. 49°-59° C., which appeared hygroscopic. The crude product was used for the next reaction without purification. NMR (CDCl3) δ0.90 (s, 1H, OH), 9.67 (t, 1H, J=1.5 Hz, CHO), 7.70 (d, 1H, J=3 Hz, aromatic proton), 7.23 (d, 1H, aromatic proton), 3.97 (s, 3H, CH3) and 3.70(d, 2H, CH2).

후처리

  1. stirringThe mixture was stirred at room temperature for another 21 hours
  2. customThe layers were separated
  3. extractionthe aqueous layer extracted with ethyl ether (2×400 ml)
  4. dry with materialdried over anhydrous Na2SO4
  5. filtrationfiltered through a column of Florisil (85 g)
  6. customto remove inorganic impurity
  7. customEvaporation of the ether

출처 및 근거

ORD 기록
ord-7cfa05e61b5649588371d8a8f494ed36
출처 데이터셋
uspto-grants-1992_12
특허 번호
US05175173

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