Tributyl borate → 3-(1-Carboxy-ethyl)-phenyl boronic acid

HRID 216177

反応式

HRID 216177 の反応式
Br[C:2]1[CH:3]=[C:4]([CH:8]([CH3:12])[C:9]([OH:11])=[O:10])[CH:5]=[CH:6][CH:7]=1.C([Li])(C)(C)C.[B:18](OCCCC)([O:24]CCCC)[O:19]CCCC>CCOCC>[C:9]([CH:8]([C:4]1[CH:3]=[C:2]([B:18]([OH:24])[OH:19])[CH:7]=[CH:6][CH:5]=1)[CH3:12])([OH:11])=[O:10]

参加物

5

反応物 3

HCID 12712Tributyl borateHCID 127979542-(3-Bromophenyl)propanoic acid2 回HCID 178418306HCID 178418306、化合物

生成物 1

HCID 576360703-(1-Carboxy-ethyl)-phenyl boronic acid

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

実験手順

A solution of 2-(3-bromo-phenyl)-propionic acid [500 mg, 2.18 mmol, Intermediate (69)] in anhydrous ether (20 mL) is added tert-butyl lithium (1.7 M in pentane, 5.4 mL, 9.16 mmol) dropwise at −78° C. and this mixture is stirred for 30 minutes treated with tributyl borate (2.34 mL, 8.72 mmol). The reaction mixture is allowed to warm up to room temperature, stirred for 15 hours, diluted with ether, and quenched with 1 M H3PO4. After stirring for 30 minutes the ether layer is separated and extracted three times with 2 N sodium hydroxide (20 mL). The combined sodium hydroxide extracts are acidified with 6 N hydrochloric acid to pH=1 and extracted three times with ether (50 mL). The combined organic extracts are washed with brine, dried over sodium sulfate and concentrated to obtain 3-(1-carboxy-ethyl)-phenyl boronic acid [Intermediate (70)] as a solid, which is used without further purification.

後処理

  1. stirringstirred for 15 hours
  2. customquenched with 1 M H3PO4
  3. stirringAfter stirring for 30 minutes the ether layer
  4. customis separated
  5. extractionextracted three times with 2 N sodium hydroxide (20 mL)
  6. extractionextracted three times with ether (50 mL)
  7. washThe combined organic extracts are washed with brine
  8. dry with materialdried over sodium sulfate
  9. concentrationconcentrated

出典と根拠

ORDレコード
ord-33babe47ffbc4957a900b1aba4e92a00
出典データセット
uspto-grants-2012_06
特許番号
US08193183B2

関連ノート

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