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Diisobutylaluminum hydride → HCID 86635037、化合物

HRID 1367677
ノート
印刷プレビュー

反応式

HRID 1367677 の反応式
CC(C[AlH]CC(C)C)C.C([O:12][C:13]([C@@H:15]1[CH2:19][C:18]([C:20]2[CH:25]=[CH:24][C:23](C)=[CH:22][N:21]=2)=[C:17]([CH3:27])[C@H:16]1[O:28][Si:29]([CH2:34][CH3:35])([CH2:32][CH3:33])[CH2:30][CH3:31])=O)C>C1(C)C=CC=CC=1>[CH3:27][C:17]1[C@@H:16]([O:28][Si:29]([CH2:30][CH3:31])([CH2:34][CH3:35])[CH2:32][CH3:33])[C@H:15]([CH:13]=[O:12])[CH2:19][C:18]=1[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][N:21]=1
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 2

HCID 14487Diisobutylaluminum hydrideHCID 67267363HCID 67267363、化合物

生成物 1

HCID 86635037HCID 86635037、化合物

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

A solution of DIBAL-H (0.44 ml, 1.0 M in hexane, 0.44 mmol, 1.1 equiv) was added dropwise to a solution of silyl ether 93 (150 mg, 0.4 mmol) in toluene (2 ml) at −78° C. The reaction mixture was stirred at that temperature for 1 hr and quenched by dropwise addition of saturated NH4Cl solution (0.2 ml). The reaction mixture was allowed to reach room temperature and a saturated solution of Rochelle salt (1 ml) and brine (0.4 ml) were added. The mixture was extracted with ethyl acetate (3×2 ml) and the combined organic extracts were dried over anhydrous sodium sulfate, filtered, and evaporated in vacuo to give crude aldehyde 94 as a yellow liquid which was used in the next step without further purification.

後処理

  1. customquenched by dropwise addition of saturated NH4Cl solution (0.2 ml)
  2. customto reach room temperature
  3. additiona saturated solution of Rochelle salt (1 ml) and brine (0.4 ml) were added
  4. extractionThe mixture was extracted with ethyl acetate (3×2 ml)
  5. dry with materialthe combined organic extracts were dried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. customevaporated in vacuo

出典と根拠

ORDレコード
ord-3aa433c2aab94bff9dc330abaa7d599c
出典データセット
uspto-grants-2011_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07893268B2

反応ノート

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