Estragole → Chavicol

HRID 324165

反応式

HRID 324165 の反応式
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH:10]=[CH2:11])=[CH:5][CH:4]=1.B(Br)(Br)Br.[B]>C(Cl)Cl>[CH2:9]([C:6]1[CH:7]=[CH:8][C:3]([OH:2])=[CH:4][CH:5]=1)[CH:10]=[CH2:11]

参加物

5

反応物 3

HCID 8815EstragoleHCID 25134Boron tribromideHCID 5462311Boron

生成物 1

HCID 68148Chavicol収率 56%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

To 50.01 g (337.4 mmol) of 1-methoxy-4-(2-propenyl)benzene (Aldrich Chemical Company, Milwaukee, Wis.) dissolved in 300 mL of anhydrous methylene chloride was added dropwise 375 mL (375 mmol) of 1.0 M boron tribromide (Aldrich) in methylene chloride. The reaction was run under nitrogen at room temperature and the mixture was stirred for 1 hour. The mixture was poured over 1000 mL of crushed ice, stirred for 5 minutes, and transferred to a separatory funnel. The organic layer was drained and saved. The boron salts were transferred to a filter containing Celite™ (Aldrich Chemical Co., Milwaukee, Wis.) and the filter containing the salts was washed with portions of methylene chloride and then water. The filtrate was transferred to a separatory funnel and the organic and aqueous layers were separated. The aqueous layer was extracted with four 100mL portions of methylene chloride. The methylene chloride solutions were pooled, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under vacuum to yield 25.27 g (56%) of crude 4-(2-propenyl)phenol. The crude product was distilled twice at reduced pressure to yield 20.34 g (45%) of 4-(2-propenyl)phenol. The NMR data was consistent with that reported by Rajashekhar and coworkers (J. Biol. Chem. 1984, 259, 6925).

後処理

  1. customwas run under nitrogen at room temperature
  2. stirringstirred for 5 minutes
  3. customtransferred to a separatory funnel
  4. additioncontaining Celite™ (Aldrich Chemical Co., Milwaukee, Wis.)
  5. additionthe filter containing the salts
  6. washwas washed with portions of methylene chloride
  7. customThe filtrate was transferred to a separatory funnel
  8. customthe organic and aqueous layers were separated
  9. extractionThe aqueous layer was extracted with four 100mL portions of methylene chloride
  10. dry with materialdried over anhydrous magnesium sulfate
  11. filtrationfiltered
  12. customThe solvent was removed under vacuum

出典と根拠

ORDレコード
ord-b83cc61268e241909530bbd1cfaf840c
出典データセット
uspto-grants-2001_04
特許番号
US06217943B1

関連ノート

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