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Dichloromethane → Benzeneacetic acid, 2,6-difluoro-4-hydroxy-, methyl ester

HRID 1474724
ノート
印刷プレビュー

反応式

HRID 1474724 の反応式
[F:1][C:2]1[CH:7]=[C:6]([O:8]C)[CH:5]=[C:4]([F:10])[C:3]=1[CH2:11][C:12]([OH:14])=[O:13].B(Br)(Br)Br.Cl[CH2:20]Cl>>[F:1][C:2]1[CH:7]=[C:6]([OH:8])[CH:5]=[C:4]([F:10])[C:3]=1[CH2:11][C:12]([O:14][CH3:20])=[O:13]
参加物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 6344Dichloromethane2 回HCID 25134Boron tribromideHCID 51873792-(2,6-Difluoro-4-methoxyphenyl)acetic acid

生成物 1

HCID 68228239Benzeneacetic acid, 2,6-difluoro-4-hydroxy-, methyl ester

実験手順

To a stirred solution of (2,6-difluoro-4-methoxyphenyl)acetic acid (1.50 g, 7.42 mmol) in 20 ml anhydrous dichloromethane at 0° C. was added a solution of boron tribromide (4.29 ml, 44.5 mmol) in 10 ml anhydrous dichloromethane. The cooling bath was removed and the mixture allowed to warm to RT for 2 hours. The reaction was diluted with 20 ml anhydrous methanol, and stirred for 30 minutes. The mixture was concentrated under reduced pressure, and the residue purified by column chromatography on silica gel, (Biotage column, 50 g) using a gradient eluent of 0-30% ethyl acetate in hexanes (700 ml) to afford the title compound. 1H NMR (CDCl3): δ 6.30 (d, J=8.3 Hz, 2H), 6.12 (br, 1H), 3.76 (s, 3H), 3.63 (s, 2H).

後処理

  1. customThe cooling bath was removed
  2. additionThe reaction was diluted with 20 ml anhydrous methanol
  3. concentrationThe mixture was concentrated under reduced pressure
  4. customthe residue purified by column chromatography on silica gel, (Biotage column, 50 g)

出典と根拠

ORDレコード
ord-b9a8b9c3000b42259b648604ce95a09a
出典データセット
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09018224B2

反応ノート

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