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

HRID 222567

反応式

HRID 222567 の反応式
[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

参加物

5

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 24193Titanium Tetrachloride触媒HCID 6344Dichloromethane溶媒2 回

実験手順

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).

後処理

  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)]

出典と根拠

ORDレコード
ord-d34750365c044735ae4ce4e50a86943a
出典データセット
uspto-grants-2012_06
特許番号
US08207329B2

関連ノート

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