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Triethylamine → HCID 23501331、化合物

HRID 703704
ノート
印刷プレビュー

反応式

HRID 703704 の反応式
C(N(CC)CC)C.[O:8]([C:16]1[CH:17]=[C:18]([CH:23]=[CH:24][CH:25]=1)[C:19]([O:21][CH3:22])=O)[Si:9]([C:12]([CH3:15])([CH3:14])[CH3:13])([CH3:11])[CH3:10].[CH:26]12[CH2:35][CH:30]3[CH2:31][CH:32]([CH2:34][CH:28]([CH2:29]3)[C:27]1=O)[CH2:33]2>O.C1COCC1.CCCCCC.[Cl-].[Cl-].[Cl-].[Ti+3].[Zn]>[Si:9]([O:8][C:16]1[CH:17]=[C:18]([CH2:19][O:21][CH:22]=[C:27]2[CH:28]3[CH2:34][CH:32]4[CH2:31][CH:30]([CH2:35][CH:26]2[CH2:33]4)[CH2:29]3)[CH:23]=[CH:24][CH:25]=1)([C:12]([CH3:15])([CH3:14])[CH3:13])([CH3:11])[CH3:10]
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 3

HCID 8471Triethylamine2 回HCID 64151AdamantanoneHCID 11715937Benzoic acid, 3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-, methyl ester

生成物 1

HCID 23501331HCID 23501331、化合物収率 82.2%

試薬・触媒・溶媒 5

HCID 23994Zinc触媒
HCID 10313229
titanium(III) trichloride
触媒
HCID 962Water溶媒
HCID 8028Tetrahydrofuran溶媒2 回
HCID 8058Hexane溶媒

実験手順

To a four-necked round-bottom flask equipped with a refluxing condenser and mechanical stirrer was added 1.5 L of dry THF under argon. Titanium trichloride (TiCl3, 200 g, 1.29 mol) was then added to the flask with stirring. After 15 minutes of stirring, powdered zinc (130 g, 2.0 mol) was added in portions and the flask was heated in hot water for 25 minutes. The reaction flask was then cooled in an ice-salt bath and the temperature of the mixture maintained at 5° to 7° C. Triethylamine (2.0 mL) was added to the suspension with caution (the reaction is extremely exothermic). The reaction started in approximately 5 to 10 minutes. After the reaction subsided, an additional amount of triethylamine (200 mL) was added and the mixture heated under reflux for 3 hours. After this period, a solution of methyl 3-tert-butyldimethylsiloxybenzoate (100 g, 0.37 mol) and 2-adamantanone (85.0 g, 0.57 mol) in 400 mL of dry THF was added dropwise to the refluxing mixture over 5 hours. The reaction mixture was then cooled to room temperature and was diluted with hexane (4 L) and the stirring continued. The suspended solids were then allowed to settle and the organic layer decanted. The black solid was washed with diethyl ether (2×1 L). Hexane (1 L) was added to the black material, followed by 1 L of water and the organic layer was removed. The aqueous layer was washed a second time with 1.5 L of hexane. The combined hexane and ether layers were then gravity filtered and the resulting solution was dried over anhydrous magnesium sulfate. Evaporation of the solvent under reduced pressure and chromatography over silica gel with 5% ethyl acetate/hexane gave 117 g (81% yield) of 2 as a clear oil.

後処理

  1. customTo a four-necked round-bottom flask equipped with a refluxing condenser and mechanical stirrer
  2. stirringAfter 15 minutes of stirring
  3. temperatureThe reaction flask was then cooled in an ice-salt bath
  4. temperaturethe temperature of the mixture maintained at 5° to 7° C
  5. temperaturethe mixture heated
  6. temperatureunder reflux for 3 hours
  7. waitAfter this period
  8. customthe organic layer decanted
  9. washThe black solid was washed with diethyl ether (2×1 L)
  10. additionHexane (1 L) was added to the black material
  11. customthe organic layer was removed
  12. washThe aqueous layer was washed a second time with 1.5 L of hexane
  13. filtrationgravity filtered
  14. dry with materialthe resulting solution was dried over anhydrous magnesium sulfate
  15. customEvaporation of the solvent under reduced pressure and chromatography over silica gel with 5% ethyl acetate/hexane

出典と根拠

ORDレコード
ord-9dcce1f30b2d4f7e9c03dd41fa9ccbbe
出典データセット
uspto-grants-1991_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04983779

反応ノート

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