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Hydrochloric Acid → (1-methyl-1H-pyrazol-5-yl)boronic acid

HRID 46337
ノート
印刷プレビュー

反応式

HRID 46337 の反応式
[CH3:1][N:2]1[CH:6]=[CH:5][CH:4]=[N:3]1.C([Li])CCC.[B:12](OC(C)C)([O:17]C(C)C)[O:13]C(C)C.Cl>O1CCCC1>[CH3:1][N:2]1[C:6]([B:12]([OH:17])[OH:13])=[CH:5][CH:4]=[N:3]1
参加物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 313Hydrochloric AcidHCID 21531Triisopropyl borateHCID 702551H-Pyrazole, 1-methyl-HCID 178418339Butyllithium

生成物 1

HCID 11182610(1-methyl-1H-pyrazol-5-yl)boronic acid収率 33%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

To a stirred solution of 1-methyl-1H-pyrazole (2.49 mL, 30 mmol) in tetrahydrofuran (100 mL) was added butyllithium (2.5 M in hexane, 15.6 mL, 39 mmol) at −78° C. dropwise. After stirring for 1 hour, triisopropyl borate (27.6 mL, 120 mmol) was added and the reaction mixture was gradually warmed to room temperature for 16 hours. Hydrochloric acid (1 N aqueous solution) was added to the reaction mixture until pH 7 achieved. The mixture was extracted with dichloromethane:methanol (9:1, 5×200 mL). Combined organic extracts were dried over magnesium sulphate and concentrated in vacuo to obtain crude residue. Purification was undertaken by flash column chromatography (ISCO™) eluting with dichloromethane:methanol (7:3, by volume) to afford the title compound as a white solid, 1258 mg, 33% yield.

後処理

  1. extractionThe mixture was extracted with dichloromethane:methanol (9:1, 5×200 mL)
  2. dry with materialCombined organic extracts were dried over magnesium sulphate
  3. concentrationconcentrated in vacuo
  4. customto obtain crude residue
  5. customPurification
  6. washeluting with dichloromethane:methanol (7:3, by volume)

出典と根拠

ORDレコード
ord-d10a93e5238f4cc7a481ac6945dcec4e
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08541588B2

反応ノート

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