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Methyl iodide → (2,2-Difluoro-7-methyl-1,3-benzodioxol-4-yl)boronic acid

HRID 527655
ノート
印刷プレビュー

反応式

HRID 527655 の反応式
[F:1][C:2]1([F:14])[O:6][C:5]2[CH:7]=[CH:8][CH:9]=[C:10]([B:11]([OH:13])[OH:12])[C:4]=2[O:3]1.[Li][CH:16](CC)C.C1CCCCC1.CI>C1COCC1>[F:14][C:2]1([F:1])[O:6][C:5]2[C:7]([CH3:16])=[CH:8][CH:9]=[C:10]([B:11]([OH:13])[OH:12])[C:4]=2[O:3]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

6

反応物 4

HCID 6328Methyl iodideHCID 8078CyclohexaneHCID 16427145(2,2-Difluoro-1,3-dioxaindan-4-yl)boronic acid2 回HCID 178418400CID 53628100

生成物 1

HCID 86698459(2,2-Difluoro-7-methyl-1,3-benzodioxol-4-yl)boronic acid

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
-78 °C

実験手順

(2,2-difluoro-1,3-benzodioxol-4-yl)boronic acid (Intermediate 195, crude material) was dissolved in THF (20 mL) and the resulting solution cooled down to −78° C. sec-BuLi 1.4M solution in cyclohexane (17.4 ml, 24.36 mmol) was added dropwise and the reaction mixture was stirred for 1.5 hours at −78° C. Methyl iodide (4.6 ml, 73 mmol) was then added and the reaction mixture was stirred for 2 hours while the temperature was allowed to reach room temperature. The reaction was quenched by addition of an aqueous 2N solution of HCl and diluted with ethyl acetate. The organic layer was collected and then washed twice with brine, dried over Na2SO4 and evaporated to dryness. Crystallization from n-heptane afforded the title compound (150 mg) as white solid.

後処理

  1. additionwas added dropwise
  2. stirringthe reaction mixture was stirred for 2 hours while the temperature
  3. customto reach room temperature
  4. customThe reaction was quenched by addition of an aqueous 2N solution of HCl
  5. additiondiluted with ethyl acetate
  6. customThe organic layer was collected
  7. washwashed twice with brine
  8. dry with materialdried over Na2SO4
  9. customevaporated to dryness
  10. customCrystallization from n-heptane

出典と根拠

ORDレコード
ord-d2f505d1d255450a8c5eb99f499f23f2
出典データセット
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09346790B2

反応ノート

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