Trimethyl borate → (6-Phenyldibenzo[b,d]furan-4-yl)boronic acid

HRID 717995

反応式

HRID 717995 の反応式
C([Li])CCC.[C:6]1([C:12]2[C:17]3[O:18][C:19]4[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=4[C:16]=3[CH:15]=[CH:14][CH:13]=2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[B:25](OC)([O:28]C)[O:26]C.[NH4+].[OH-]>C1COCC1>[C:6]1([C:12]2[C:17]3[O:18][C:19]4[C:24]([B:25]([OH:28])[OH:26])=[CH:23][CH:22]=[CH:21][C:20]=4[C:16]=3[CH:15]=[CH:14][CH:13]=2)[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=1

参加物

6

反応物 4

HCID 8470Trimethyl borateHCID 14923Ammonium HydroxideHCID 64257504-PhenyldibenzofuranHCID 178418339Butyllithium

生成物 1

HCID 89556926(6-Phenyldibenzo[b,d]furan-4-yl)boronic acid収率 85%

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

実験手順

n-Butyllithium (13.51 mL, 33.8 mmol) was added dropwise to 4-phenyldibenzo[b,d]furan (3.3 g, 13.51 mmol) in 80 mL dry THF at −78° C. This reaction mixture was allowed to stir at room temperature for 5 hours and then cooled to −78° C. again. Trimethyl borate (4.52 mL, 40.5 mmol) was added slowly to the reaction. The reaction mixture was allowed to warm up to room temperature gradually over night with stirring. The mixture was poured into 50 mL of NH4OH solution with ice. The aqueous mixture was extracted with 3×80 mL ethyl acetate and dried over sodium sulfate, and the organic layer was evaporated to get yield 3.3 g (85%) product, which was used without purification and was confirmed by NMR.

後処理

  1. temperaturecooled to −78° C. again
  2. temperatureto warm up to room temperature gradually over night
  3. stirringwith stirring
  4. extractionThe aqueous mixture was extracted with 3×80 mL ethyl acetate
  5. dry with materialdried over sodium sulfate
  6. customthe organic layer was evaporated

出典と根拠

ORDレコード
ord-d772e11d94504c63bfd97bfe1f6ec880
出典データセット
uspto-grants-2015_11
特許番号
US09193745B2

関連ノート

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