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Ethanol → HCID 10590086、化合物

HRID 1781456
ノート
印刷プレビュー

反応式

HRID 1781456 の反応式
P(Br)(Br)[Br:2].[CH:5]([C:8]1[CH:15]=[C:14]([CH:16]([CH3:18])[CH3:17])[CH:13]=[C:12]([CH:19]([CH3:21])[CH3:20])[C:9]=1[CH2:10]O)([CH3:7])[CH3:6].CCO>CCOCC>[CH:5]([C:8]1[CH:15]=[C:14]([CH:16]([CH3:18])[CH3:17])[CH:13]=[C:12]([CH:19]([CH3:21])[CH3:20])[C:9]=1[CH2:10][Br:2])([CH3:7])[CH3:6]
参加物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 702EthanolHCID 24614Phosphorus tribromideHCID 10728422HCID 10728422、化合物

生成物 1

HCID 10590086HCID 10590086、化合物

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

実験手順

A solution of PBr3 (2.7 9, 10 mmol) in ether (10 mL) was added slowly to a solution of 2,4,6-triisopropylbenzyl alcohol (4.68 9, 20 mmol) in 20 mL of ether at room temperature. The mixture was stirred for 1 hour, 5 mL of absolute EtOH was added, and stirring was continued for another 0.5 hour. The solvent was removed and the residue distributed between EtOAc and saturated Na2CO3. The EtOAc layer was separated, washed with brine, and dried over MgSO4. The solvent was evaporated and the pure product was isolated by column chromatography (100% CH2Cl2, 3.5 g, 59%); NMR (CDCl3):δ 1.2-1.4 (m, 18H), 2.8-3.0 (m, 1H), 3.2-3.45 (m, 2H), 4.7 (s, 2H), 7.04 (s, 2H) ppm.

後処理

  1. stirringstirring
  2. waitwas continued for another 0.5 hour
  3. customThe solvent was removed
  4. customThe EtOAc layer was separated
  5. washwashed with brine
  6. dry with materialdried over MgSO4
  7. customThe solvent was evaporated
  8. customthe pure product was isolated by column chromatography (100% CH2Cl2, 3.5 g, 59%)

出典と根拠

ORDレコード
ord-9d7460f0cb01456c9721e72993467fc8
出典データセット
uspto-grants-1997_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05633287

反応ノート

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