Water → 5-Bromo-2-chloro-4-(methoxycarbonyl)benzoic acid

HRID 1716955ノート

反応式

HRID 1716955 の反応式
[Br:1][C:2]1[CH:11]=[C:10]([CH3:12])[C:9]([Cl:13])=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].C1OCCOCCOCCOCCOCC[O:16]C1.C(O)(C)(C)C.[OH2:37]>>[Br:1][C:2]1[C:3]([C:4]([O:6][CH3:7])=[O:5])=[CH:8][C:9]([Cl:13])=[C:10]([CH:11]=1)[C:12]([OH:16])=[O:37]

参加物

5

反応条件

温度
55 °C

実験手順

A mixture of methyl 2-bromo-5-chloro-4-methylbenzoate (39.53 g, 0.15 mol), 18-Crown-6 (3.95 g), tert-butyl alcohol (350 mL), and water (750 mL) was combined together with mechanical stirring. The reaction mixture was heated to reflux and monitored by TLC. After refluxing overnight, the reaction was cooled to 55° C. and filtered. The filter cake was washed with hot water (2×100 mL, 50° C.). The filtrate was neutralized with 18% hydrochloric acid to pH 1 and stored in refrigerator (0˜5° C.) for 3 h. It was filtered, washed with ice water (2×50 mL) and petroleum ether (2×50 mL). The filter cake was dried under vacuum to give the title compound as a white crystalline. Yield: 32.1 g (73%). 1H NMR (DMSO-d6, 300 MHz): δ 8.10 (s, 1H), 7.89 (s, 1H), 3.86 (s, 3H).

後処理

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux
  3. temperatureAfter refluxing overnight
  4. filtrationfiltered
  5. washThe filter cake was washed with hot water (2×100 mL, 50° C.)
  6. filtrationIt was filtered
  7. washwashed with ice water (2×50 mL) and petroleum ether (2×50 mL)
  8. customThe filter cake was dried under vacuum

出典と根拠

ORDレコード
ord-5c12185339984e0c81e382300fb1c918
出典データセット
uspto-grants-2010_09
特許番号
US07803778B2

反応ノート

読み込み中…