Silane, trimethyl((1-methylethenyl)oxy)- → 7-(tert-Butyldiphenylsilyloxy)4-[3-(tert-butyldiphenylsilyloxy)propyl]-4-hydroxyheptan-2-one

HRID 222567

반응식

HRID 222567 반응식
[Si:1]([O:18][CH2:19][CH2:20][CH2:21][C:22](=[O:44])[CH2:23][CH2:24][CH2:25][O:26][Si:27]([C:40]([CH3:43])([CH3:42])[CH3:41])([C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1)[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)([C:14]([CH3:17])([CH3:16])[CH3:15])([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C[Si](C)(C)[O:47][C:48]([CH3:50])=[CH2:49]>C(Cl)Cl.Cl[Ti](Cl)(Cl)Cl>[Si:1]([O:18][CH2:19][CH2:20][CH2:21][C:22]([CH2:23][CH2:24][CH2:25][O:26][Si:27]([C:40]([CH3:43])([CH3:42])[CH3:41])([C:34]1[CH:35]=[CH:36][CH:37]=[CH:38][CH:39]=1)[C:28]1[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=1)([OH:44])[CH2:49][C:48](=[O:47])[CH3:50])([C:14]([CH3:15])([CH3:16])[CH3:17])([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

참가 물질

5

반응물 2

HCID 74599Silane, trimethyl((1-methylethenyl)oxy)-HCID 689819261,7-Bis(tert-butyldiphenylsilyloxy)heptan-4-one

생성물 1

HCID 689834157-(tert-Butyldiphenylsilyloxy)4-[3-(tert-butyldiphenylsilyloxy)propyl]-4-hydroxyheptan-2-one수율 10.3%

시약·촉매·용매 2

HCID 24193Titanium Tetrachloride촉매HCID 6344Dichloromethane용매2회

실험 절차

A solution of 50 (160 mg, 0.257 mmol) in anhydrous CH2Cl2 (0.3 mL) was cooled in an ice bath under argon for 10 min. TiCl4 (25 μL) was added, and the resulting mixture was stirred for 10 min. 2-(Trimethylsilyloxy)prop-1-ene (33.4 mg, 0.257 mmol, 0.43 μL) was added. Stirring was continued for 20 min. The reaction mixture was diluted with ice-cold water. CH2Cl2 was added, and the phases were separated. The aqueous layer was extracted with CH2Cl2. The combined organic layers were dried (Na2SO4). Concentration of the sample under reduced pressure yielded a pale yellow oil, which was purified by column chromatography [silica, hexanes/ethyl acetate (10:1→3:1)] affording a colorless oil (18 mg, 10%): 1H NMR δ 1.04 (s, 18H), 1.85-1.89 (m, 4H), 2.18 (s, 3H), 2.61 (s, 2H), 3.65 (m, 4H), 7.37-6.42 (m, 12H), 7.65-7.67 (m, 8H).

후처리

  1. stirringStirring
  2. waitwas continued for 20 min
  3. additionThe reaction mixture was diluted with ice-cold water
  4. customthe phases were separated
  5. extractionThe aqueous layer was extracted with CH2Cl2
  6. dry with materialThe combined organic layers were dried (Na2SO4)
  7. customConcentration of the sample under reduced pressure yielded a pale yellow oil, which
  8. customwas purified by column chromatography [silica, hexanes/ethyl acetate (10:1→3:1)]

출처 및 근거

ORD 기록
ord-d34750365c044735ae4ce4e50a86943a
출처 데이터셋
uspto-grants-2012_06
특허 번호
US08207329B2

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