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

Methanol → Methyl 4-bromo-2-fluoro-5-methylbenzoate

HRID 508188
ノート
印刷プレビュー

反応式

HRID 508188 の反応式
[Br:1][C:2]1[C:10]([CH3:11])=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4]([F:12])[CH:3]=1.O=S(Cl)Cl.[CH3:17]O>>[Br:1][C:2]1[C:10]([CH3:11])=[CH:9][C:5]([C:6]([O:8][CH3:17])=[O:7])=[C:4]([F:12])[CH:3]=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

4

反応物 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 341745874-Bromo-2-fluoro-5-methylbenzoic acid

生成物 1

HCID 66817979Methyl 4-bromo-2-fluoro-5-methylbenzoate

反応条件

温度
80 °C

実験手順

To a solution of 4-bromo-2-fluoro-5-methylbenzoic acid (i-2a) (1.87 g, 8 mmol) in CH3OH (50 mL) at 0° C. was added SOCl2 (6 mL, 80 mmol) dropwise. Then the mixture was heated to 80° C. for 2 h. The solvent was removed in vacuo and the residue was diluted with EtOAc and washed with H2O, brine, dried over anhydrous Na2SO4, and concentrated. The resulting crude solid was washed with PE to give the title compound as a yellow solid. 1H NMR (400 MHz, CDCl3) δ 7.80 (1H, d), 7.37 (1H, d), 3.92 (3H, s), 2.39 (3H, s).

後処理

  1. customThe solvent was removed in vacuo
  2. additionthe residue was diluted with EtOAc
  3. washwashed with H2O, brine
  4. dry with materialdried over anhydrous Na2SO4
  5. concentrationconcentrated
  6. washThe resulting crude solid was washed with PE

出典と根拠

ORDレコード
ord-41752e8eda6a478d996396309c9f08f6
出典データセット
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09095583B2

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