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Dimethyl Sulfate → 2,6-Dimethyl-2-methoxyhept-5-ene

HRID 329470
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HRID 329470 반응식
[H-].[Na+].[CH3:3][C:4]([OH:12])([CH2:6][CH2:7][CH:8]=[C:9]([CH3:11])[CH3:10])[CH3:5].[CH3:13]OS(OC)(=O)=O>O1CCCC1>[CH3:3][C:4]([O:12][CH3:13])([CH2:6][CH2:7][CH:8]=[C:9]([CH3:11])[CH3:10])[CH3:5]
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참가 물질

5

반응물 3

HCID 6497Dimethyl SulfateHCID 24758Sodium hydrideHCID 801835-Hepten-2-ol, 2,6-dimethyl-

생성물 1

HCID 147939932,6-Dimethyl-2-methoxyhept-5-ene

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매3회

실험 절차

To sodium hydride (93.5 g, 3.9 mol) suspended in tetrahydrofuran (300 mL) was added 2,6-dimethylhept-5-en-2-ol (500 g, 3.5 mol) in tetrahydrofuran (1000 mL). The mixture was heated at reflux until gas evolution was complete. Dimethylsulfate (274 mL, 2.9 mol) in tetrahydrofuran (226 mL) was added to the cold (0° C.) mixture. After standing for 16 h, the mixture was heated at reflux for 7 hours. Aqueous workup yielded 2,6-dimethyl-2-methoxyhept-5-ene, bp40 65°-68° C. (461.5 g); NMR(CDCl3)δ1.2(s,6H), 1.4-1.6(m,2H), 1.6(s,3H), 1.7(s,3H), 1.9-2.1(m,2H), 3.2(s,3H), 5.1-5.2(m,1H); IR(neat) 2970, 2932, 1462, 1442, 1373, 1357, 1195, 1072 cm-1 ; MS(m/e) 41, 67, 73, 109, 124, 142.

후처리

  1. temperatureThe mixture was heated
  2. temperatureat reflux until gas evolution
  3. temperaturethe mixture was heated
  4. temperatureat reflux for 7 hours

출처 및 근거

ORD 기록
ord-0b58e511358c450b9ce218a85e8f3b8a
출처 데이터셋
uspto-grants-1990_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04891447

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