Water → HCID 58559582、化合物

HRID 1478956ノート

反応式

HRID 1478956 の反応式
[Br-:1].[Mg+2].[Br-].S(O[CH2:9][CH2:10][CH2:11][CH2:12][CH2:13]/[CH:14]=[CH:15]\[CH2:16]/[CH:17]=[CH:18]\[CH2:19]/[CH:20]=[CH:21]\[CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])(=O)(=O)C.O>CCOCC>[CH2:9]([Br:1])[CH2:10][CH2:11][CH2:12][CH2:13]/[CH:14]=[CH:15]\[CH2:16]/[CH:17]=[CH:18]\[CH2:19]/[CH:20]=[CH:21]\[CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]

参加物

5

実験手順

Magnesium bromide etherate (34 g, 110 mmol) and a stir bar were added to a 2000 mL round bottom flask. The flask was sealed and flushed with nitrogen. Anhydrous diethyl ether (400 mL) was added via canulla. A solution of γ-linolenyl mesylate (20 g, 58 mmol) in anhydrous ether (300 mL) was then added, and the suspension stirred overnight. The suspension was poured into 500 mL of chilled water and transferred to a 2000-mL separating funnel. After shaking, the organic phase was separated. The aqueous phase was then extracted with ether (2×250 mL) and all ether phases combined. The ether phase was washed with water (2×250 mL), brine (250 mL) and dried over anhydrous Mg2SO4. The solution was filtered, concentrated and purified by flash chromatography. Final yield 18.9 g, 99%.

後処理

  1. customThe flask was sealed
  2. customflushed with nitrogen
  3. additionAnhydrous diethyl ether (400 mL) was added via canulla
  4. customseparating funnel
  5. stirringAfter shaking
  6. customthe organic phase was separated
  7. extractionThe aqueous phase was then extracted with ether (2×250 mL)
  8. washThe ether phase was washed with water (2×250 mL), brine (250 mL)
  9. dry with materialdried over anhydrous Mg2SO4
  10. filtrationThe solution was filtered
  11. concentrationconcentrated
  12. custompurified by flash chromatography

出典と根拠

ORDレコード
ord-2441aaee188e4825ac2612c60ddf1dda
出典データセット
uspto-grants-2016_08
特許番号
US09404127B2

反応ノート

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