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Diisopropylamine → (+)-3-(Benzyloxy)-6(8-hydroxy-1,4-dioxaspiro[4.5]dec-8-yl)-2-cyclohexen-1-one

HRID 23599
ノート
印刷プレビュー

反応式

HRID 23599 の反応式
C(NC(C)C)(C)C.C([Li])CCC.[CH2:13]([O:20][C:21]1[CH2:26][CH2:25][CH2:24][C:23](=[O:27])[CH:22]=1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.[CH2:28]1[O:38][C:31]2([CH2:36][CH2:35][C:34](=[O:37])[CH2:33][CH2:32]2)[O:30][CH2:29]1.[Cl-].[NH4+]>O1CCCC1.ClCCl>[CH2:13]([O:20][C:21]1[CH2:26][CH2:25][CH:24]([C:34]2([OH:37])[CH2:35][CH2:36][C:31]3([O:38][CH2:28][CH2:29][O:30]3)[CH2:32][CH2:33]2)[C:23](=[O:27])[CH:22]=1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 7912DiisopropylamineHCID 25517Ammonium ChlorideHCID 5674151,4-Dioxaspiro[4.5]decan-8-oneHCID 108889653-Benzyloxy-2-cyclohexen-1-oneHCID 178418339Butyllithium

生成物 1

HCID 12992125(+)-3-(Benzyloxy)-6(8-hydroxy-1,4-dioxaspiro[4.5]dec-8-yl)-2-cyclohexen-1-one収率 88.2%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 8028Tetrahydrofuran溶媒3 回

反応条件

温度
-78 °C

実験手順

To a flask equipped with magnetic stirrer was added tetrahydrofuran (600 ml) and diisopropylamine (38.1 ml, 272 mmol). The stirred solution was cooled to −78° C. and n-butyl lithium (113.4 ml, 272 mmol, 2.4 M in hexanes) was added dropwise via syringe. The resulting yellow solution was stirred for 35 min at −78° C., then 3-(benzyloxy)-2-cyclohexen-1-one (50.0 g, 248 mmol) was added as a solution in tetrahydrofuran (100 ml). The solution was stirred for 1 hr prior to the addition of cyclohexane-1,4-dione monoethylene ketal (38.7 g, 248 mmol) as a solution in anhydrous tetrahydrofuran (100 ml). The solution was stirred for 2 hr at −78° C., then allowed to warm slowly to room temperature over 1 hr. Saturated aqueous ammonium chloride (80 ml) was added, followed by dichloromethane (700 ml) and the mixture stirred until no solids remained. The layers were separated and the aqueous phase extracted with dichloromethane (2×100 ml). The combined organic layers were washed with brine (50 ml), dried over magnesium sulfate, then concentrated in vacuo. Trituration of the resulting solid with methanol afforded the title compound (78.4 g, 88%). m/z (ES+) 359 (M+H+).

後処理

  1. customTo a flask equipped with magnetic stirrer
  2. stirringThe solution was stirred for 1 hr
  3. stirringThe solution was stirred for 2 hr at −78° C.
  4. temperatureto warm slowly to room temperature over 1 hr
  5. stirringthe mixture stirred until no solids
  6. customThe layers were separated
  7. extractionthe aqueous phase extracted with dichloromethane (2×100 ml)
  8. washThe combined organic layers were washed with brine (50 ml)
  9. dry with materialdried over magnesium sulfate
  10. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-b5c688eeb358459aa2276d064afa4f03
出典データセット
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06852747B2

反応ノート

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