Water → HCID 59643026、化合物

HRID 2251614ノート

反応式

HRID 2251614 の反応式
[CH:1]([C:4]1[CH:5]=[C:6]([O:18]C)[C:7]([O:14]COC)=[C:8]([CH:13]=1)[C:9]([O:11]C)=[O:10])([CH3:3])[CH3:2].B(Br)(Br)Br.O>C(Cl)Cl.CC(O)=O.Br>[OH:14][C:7]1[C:6]([OH:18])=[CH:5][C:4]([CH:1]([CH3:3])[CH3:2])=[CH:13][C:8]=1[C:9]([OH:11])=[O:10]

参加物

7

反応条件

温度
-70 °C

実験手順

To a solution of methyl 5-Isopropyl-3-methoxy-2-methoxymethoxy-benzoate in 5 mL dry CH2Cl2 cooled to −80° C., BBr3 (3.4 mL of a 1 m solution in CH2Cl2) was added dropwise via a syringe. The mixture was then stirred 30 min. at −70° C., then the cooling bath was removed and the stirring continued at r.t. for 1 h. The reaction was the quenched by addition of H2O and the resulting mixture was extracted twice with 30 mL CH2Cl2. The combined organic fractions were dried over MgSO4 and evaporated in vacuo to yield a brown solid. This material was redissolved in 1 mL AcOH to which 2.5 mL HBr (33% in AcOH) was added The mixture was stirred at 120° C. for 5 h, then H2O was slowly added and the mixture was extracted with EtOAc. The organic layer was washed twice with saturated NaCl solution, dried over MgSO4 and evaporated in vacuo to yield the desired product as a brown solid.

後処理

  1. customthe cooling bath was removed
  2. waitthe stirring continued at r.t. for 1 h
  3. customquenched by addition of H2O
  4. extractionthe resulting mixture was extracted twice with 30 mL CH2Cl2
  5. dry with materialThe combined organic fractions were dried over MgSO4
  6. customevaporated in vacuo
  7. customto yield a brown solid
  8. additionwas added The mixture
  9. stirringwas stirred at 120° C. for 5 h
  10. extractionthe mixture was extracted with EtOAc
  11. washThe organic layer was washed twice with saturated NaCl solution
  12. dry with materialdried over MgSO4
  13. customevaporated in vacuo

出典と根拠

ORDレコード
ord-3c697cc4ae7d417fa5ffed3abf11cc5c
出典データセット
uspto-grants-2008_01
特許番号
US07319101B2

反応ノート

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