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Diisobutylaluminumhydride → HCID 69922788、化合物

HRID 2416546
ノート
印刷プレビュー

反応式

HRID 2416546 の反応式
[H-].C([Al+]CC(C)C)C(C)C.C([O:13][C:14](=O)/[CH:15]=[C:16](/[C:18]1[CH:23]=[CH:22][C:21]([C:24]2[N:29]=[CH:28][CH:27]=[CH:26][N:25]=2)=[CH:20][CH:19]=1)\[CH3:17])C>C(Cl)Cl>[N:25]1[CH:26]=[CH:27][CH:28]=[N:29][C:24]=1[C:21]1[CH:22]=[CH:23][C:18](/[C:16](/[CH3:17])=[CH:15]/[CH2:14][OH:13])=[CH:19][CH:20]=1
参加物反応条件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 21225700DiisobutylaluminumhydrideHCID 69922546HCID 69922546、化合物

生成物 1

HCID 69922788HCID 69922788、化合物収率 87.2%

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
0 °C

実験手順

Diisobutylaluminum hydride (1.0 M solution in THF, 3.4 mL, 3.40 mmol) was added dropwise to a 0° C. solution of the product from step A (300 mg, 1.12 mmol) in methylene chloride (10 mL). The resulting solution was stirred for 20 min at 0° C., quenched with methanol (0.2 mL) followed by 15% aq. Rochelle salt (20 mL) and dichloromethane (10 mL), and allowed to stir at room temperature for 18 h. The layers were separated and the aqueous layer was extracted with methylene chloride (10 mL). The combined organic layers were washed with brine (20 mL), dried (MgSO4), and concentrated. Purification by chromatography (SiO2, 3:2 hexane/ethyl acetate) provided 221 mg (87%) of the title compound as an off-white solid. MS 227 (M+H)+.

後処理

  1. customquenched with methanol (0.2 mL)
  2. stirringto stir at room temperature for 18 h
  3. customThe layers were separated
  4. extractionthe aqueous layer was extracted with methylene chloride (10 mL)
  5. washThe combined organic layers were washed with brine (20 mL)
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated
  8. customPurification by chromatography (SiO2, 3:2 hexane/ethyl acetate)

出典と根拠

ORDレコード
ord-37d5e432d36343e3b9356be4c16df16c
出典データセット
uspto-grants-2004_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06825170B2

反応ノート

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