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

4-Iodotoluene → Tolylboronic acid

HRID 49420
ノート
印刷プレビュー

反応式

HRID 49420 の反応式
I[C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][CH:3]=1.C([Li])CCC.C([O:18][B:19](OCCCC)[O:20]CCCC)CCC>C(OCC)C>[CH3:8][C:5]1[CH:6]=[CH:7][C:2]([B:19]([OH:20])[OH:18])=[CH:3][CH:4]=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

5

反応物 3

HCID 122074-IodotolueneHCID 12712Tributyl borateHCID 178418339Butyllithium

生成物 1

HCID 79799Tolylboronic acid収率 85.2%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒

反応条件

温度
0 °C

実験手順

To a solution of 4-iodotoluene (35 g, 160.5 mmol) in diethyl ether (400 mL) was added n-butyllithium (2 M in pentane, 88.3 mL, 176.6 mmol) at 0° C. After stirring at 0° C. for another 15 min the solution was cooled to −60° C. and tributylborate (60.6 mL, 224.7 mmol) was added. The cooling bath was removed and the reaction allowed to heat up to room temperature. The solution was acidified with hydrochloric acid (2 N, 280 mL) and the organic phase separated off. The aqueous phase was extracted with diethyl ether 2×125 mL). The combined organic phases were extracted with sodium hydroxide (1 N, 5×50 mL). The combined aqueous extracts were acidified to give 18.6 g of the desired material.

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

後処理

  1. temperaturewas cooled to −60° C.
  2. customThe cooling bath was removed
  3. temperatureto heat up to room temperature
  4. customthe organic phase separated off
  5. extractionThe aqueous phase was extracted with diethyl ether 2×125 mL)
  6. extractionThe combined organic phases were extracted with sodium hydroxide (1 N, 5×50 mL)

出典と根拠

ORDレコード
ord-74803c53f6274e458b772a5e05af20cd
出典データセット
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06706749B2

反応ノート

読み込み中…