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Isopropanol → 4-Bromo-1-chloro-2-isopropoxybenzene

HRID 1371998
ノート
印刷プレビュー

反応式

HRID 1371998 の反応式
[C:1]1(P(C2C=CC=CC=2)C2C=CC=CC=2)[CH:6]=CC=C[CH:2]=1.CCOC(/N=N/C(OCC)=O)=O.C(O)(C)C.[Br:36][C:37]1[CH:38]=[C:39]([OH:44])[C:40]([Cl:43])=[CH:41][CH:42]=1>C(Cl)Cl>[Br:36][C:37]1[CH:42]=[CH:41][C:40]([Cl:43])=[C:39]([O:44][CH:1]([CH3:6])[CH3:2])[CH:38]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 3776IsopropanolHCID 11776TriphenylphosphineHCID 8203925-Bromo-2-chlorophenolHCID 5462977Diethyl azodicarboxylate

生成物 1

HCID 210710294-Bromo-1-chloro-2-isopropoxybenzene

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

To 1.70 g (6.5 mmol) of triphenylphosphine in 25 mL of CH2Cl2 at 0° C. was added 1.14 g (6.5 mmol) of diethylazodicarboxylate. After 10 minutes, 390 mg (6.5 mmol) of isopropanol was added, followed rapidly by 1.03 g (5.0 mmol) of 3-Bromo-6-chlorophenol. The reaction was complete within three hours, and was partitioned between ether and water. The phases were separated, and the ether phase was diluted with hexanes and washed twice with 10% aqueous methanol and once with brine. The ether/hexanes phase was dried over Na2SO4, filtered, and concentrated in vacuo to yield product as a clear oil.

後処理

  1. waitThe reaction was complete within three hours
  2. customwas partitioned between ether and water
  3. customThe phases were separated
  4. additionthe ether phase was diluted with hexanes
  5. washwashed twice with 10% aqueous methanol and once with brine
  6. dry with materialThe ether/hexanes phase was dried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customto yield product as a clear oil

出典と根拠

ORDレコード
ord-16a63f95237944259f1161f75fda48cd
出典データセット
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07157464B2

反応ノート

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