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Trimethyl borate → HCID 68670785、化合物

HRID 2071083
ノート
印刷プレビュー

反応式

HRID 2071083 の反応式
[Li]CCCC.[Br:6][C:7]1[CH:12]=[C:11]([CH:13]([O:16][CH3:17])[O:14][CH3:15])[CH:10]=[C:9](Br)[CH:8]=1.B(OC)(OC)[O:20]C>C1COCC1>[Br:6][C:7]1[CH:8]=[C:9]([OH:20])[CH:10]=[C:11]([CH:13]([O:16][CH3:17])[O:14][CH3:15])[CH:12]=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

5

反応物 3

HCID 8470Trimethyl borateHCID 190934581,3-Dibromo-5-(dimethoxymethyl)benzeneHCID 178418339Butyllithium

生成物 1

HCID 68670785HCID 68670785、化合物収率 45.4%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒2 回

反応条件

温度
-78 °C

実験手順

To a stirring solution of 23 mL of n-BuLi (1.6 M in hexanes) in 20 mL of THF at −78° C. was added 5.31 g of 1,3-dibromo-5-(dimethoxymethyl)benzene in 80 mL of THF dropwise over a period of about 55 min. After 50 min., 3.2 mL (28.7 mmol) of B(OMe)3 was added, and the solution was stirred at −78° C. for 20 min. The cold bath was removed and stirring continued with gradual warming to r.t. After 1 h, 1 N HCl (45 mL) was added, and the aqueous layer was extracted with EtOAc. The extract was washed with brine, dried over Na2SO4, filtered, and concentrated. To a stirring mixture of crude product in 70 mL of 1N NaOH at 0° C. was added 14.5 mL of H2O2 (30 wt % in H2O) dropwise. After 25 min., 5 N HCl was added to a pH=1, and EtOAc and H2O were added. The organic layer was washed with brine, dried over Na2SO4, filtered, and concentrated. Purification by flash silica gel chromatography (15% EtOAc/hexanes) provided 1.92 g of 3-bromo-5-(dimethoxymethyl)phenol as a pale yellow solid with some impurity.

後処理

  1. customThe cold bath was removed
  2. stirringstirring
  3. temperaturewith gradual warming to r.t
  4. waitAfter 1 h
  5. addition1 N HCl (45 mL) was added
  6. extractionthe aqueous layer was extracted with EtOAc
  7. washThe extract was washed with brine
  8. dry with materialdried over Na2SO4
  9. filtrationfiltered
  10. concentrationconcentrated
  11. additionTo a stirring mixture of crude product in 70 mL of 1N NaOH at 0° C.
  12. additionwas added 14.5 mL of H2O2 (30 wt % in H2O) dropwise
  13. waitAfter 25 min.
  14. addition5 N HCl was added to a pH=1, and EtOAc and H2O
  15. additionwere added
  16. washThe organic layer was washed with brine
  17. dry with materialdried over Na2SO4
  18. filtrationfiltered
  19. concentrationconcentrated
  20. customPurification by flash silica gel chromatography (15% EtOAc/hexanes)

出典と根拠

ORDレコード
ord-d1c590ecffec4775abad674201727e62
出典データセット
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08299267B2

反応ノート

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