ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Toluene → 4-(4-Methoxy-3-methylphenyl)benzoic acid

HRID 1242801
ノート
印刷プレビュー

反応式

HRID 1242801 の反応式
[CH3:1][C:2]1[CH:3]=[C:4](B(O)O)[CH:5]=[CH:6][C:7]=1[O:8][CH3:9].I[C:14]1[CH:22]=[CH:21][C:17]([C:18]([OH:20])=[O:19])=[CH:16][CH:15]=1.C(=O)([O-])[O-].[Cs+].[Cs+].C1(C)C=CC=CC=1>C(O)CCC.O>[CH3:1][C:2]1[CH:3]=[C:4]([C:14]2[CH:22]=[CH:21][C:17]([C:18]([OH:20])=[O:19])=[CH:16][CH:15]=2)[CH:5]=[CH:6][C:7]=1[O:8][CH3:9]
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

7

反応物 4

HCID 1140TolueneHCID 10796Cesium carbonateHCID 120854-Iodobenzoic acidHCID 2773487(4-Methoxy-3-methylphenyl)boronic acid

生成物 1

HCID 219394194-(4-Methoxy-3-methylphenyl)benzoic acid収率 30.3%

試薬・触媒・溶媒 2

HCID 2631-Butanol溶媒
HCID 962
Water
溶媒

反応条件

温度
80 °C

実験手順

3-Methyl-4-methoxyphenylboronic acid (542 mg) was combined with 4-iodobenzoic acid (810 mg), cesium carbonate (5.32 g), toluene (16 mL), water (8 mL) and n-butanol (4 mL). The mixture was degassed under vacuum with argon purging after which, tetrakis-triphenylphosphine palladium (38 mg) was added. The reaction was heated to 80° C. for 20 hours after which, it was cooled to room temperature and diluted with ethyl acetate (16 mL). The layers were separated and the organics were concentrated to dryness. The residue was purified on silica gel (50% to 100% ethyl acetate/hexane over 40 minutes) giving 3′-methyl-4′-methoxy-4-biphenylcarboxylic acid (240 mg). Yield=30%

後処理

  1. customThe mixture was degassed under vacuum with argon purging after which, tetrakis-triphenylphosphine palladium (38 mg)
  2. additionwas added
  3. temperaturewas cooled to room temperature
  4. additiondiluted with ethyl acetate (16 mL)
  5. customThe layers were separated
  6. concentrationthe organics were concentrated to dryness
  7. customThe residue was purified on silica gel (50% to 100% ethyl acetate/hexane over 40 minutes)

出典と根拠

ORDレコード
ord-f9d29adc889840bbb96747d0034ffe83
出典データセット
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07115741B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート