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Imidazole → HCID 18443667、化合物

HRID 459149
ノート
印刷プレビュー

反応式

HRID 459149 の反応式
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH:9]([O:13][CH3:14])[C:10]([OH:12])=[O:11])=[CH:4][C:3]=1[O:15][CH3:16].[Si:17](Cl)([C:20]([CH3:23])([CH3:22])[CH3:21])([CH3:19])[CH3:18].N1C=CN=C1.O>C(Cl)Cl.CN(C=O)C>[C:20]([Si:17]([CH3:19])([CH3:18])[O:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH:9]([O:13][CH3:14])[C:10]([OH:12])=[O:11])=[CH:4][C:3]=1[O:15][CH3:16])([CH3:23])([CH3:22])[CH3:21]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 795ImidazoleHCID 962WaterHCID 28928tert-Butyldimethylsilyl chlorideHCID 184436623-(4-Hydroxy-3-methoxyphenyl)-2-methoxypropanoic acid

生成物 1

HCID 18443667HCID 18443667、化合物

試薬・触媒・溶媒 1

HCID 22350042dichloromethane N,N-dimethylformamide溶媒

実験手順

To a solution of 3-(4-hydroxy-3-methoxy-phenyl)-2-methoxy-propionic acid (1.02 g, 4.87 mmol) in CH2Cl2-DMF (20 mL=10:1) was added tert-butyl-dimethylsilyl chloride (1.75 g, 11.68 mmol) and imidazole (0.70 g, 10.24 mmol). The resulting solution was stirred at room temperature overnight. Water (15 mL) was added, and the aqueous phase was extracted with hexanes (30 mL). The hexanes layer was washed with water (10 mL), dried (MgSO4), filtered, and concentrated. The crude product was dissolved in ethyl acetate (10 mL), and a saturated solution of K2CO3 (5 mL) was added. The resulting mixture was stirred for 2 hours at room temperature. The aqueous layer was extracted with ethyl acetate (10 mL), acidified to pH 3, and extracted again with ethyl acetate (3×10 mL). The later organic layers were combined and washed with brine (20 mL), dried (MgSO4), and concentrated to a yellow oil (1.2 g, 77%). 1H-NMR (200.15 MHz, CDCl3): δ 6.78–6.67 (m, 3H), 3.96 (dd, 1H, J=7.8, 4.0), 3.78 (s, 3H), 3.35 (s, 3H), 3.09 (dd, 1H, J=14.2, 4.0), 2.91 (dd, 1H, J=14.2, 7.8), 0.98 (s, 9H), 0.13 (6H, s).

後処理

  1. extractionthe aqueous phase was extracted with hexanes (30 mL)
  2. washThe hexanes layer was washed with water (10 mL)
  3. dry with materialdried (MgSO4)
  4. filtrationfiltered
  5. concentrationconcentrated
  6. dissolutionThe crude product was dissolved in ethyl acetate (10 mL)
  7. additiona saturated solution of K2CO3 (5 mL) was added
  8. stirringThe resulting mixture was stirred for 2 hours at room temperature
  9. extractionThe aqueous layer was extracted with ethyl acetate (10 mL)
  10. extractionextracted again with ethyl acetate (3×10 mL)
  11. washwashed with brine (20 mL)
  12. dry with materialdried (MgSO4)
  13. concentrationconcentrated to a yellow oil (1.2 g, 77%)

出典と根拠

ORDレコード
ord-a64ad25010ce46608f4c9e20881edca7
出典データセット
uspto-grants-2007_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07192982B2

反応ノート

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