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Red-Al → HCID 178484806、化合物

HRID 877008
ノート
印刷プレビュー

反応式

HRID 877008 の反応式
COCCO[AlH2-]OCCOC.[Na+].C(O[C:18]([NH:20][C@H:21]1[CH2:26][CH2:25][C@H:24]([C:27](O)=[O:28])[CH2:23][CH2:22]1)=O)(C)(C)C>C1(C)C=CC=CC=1>[CH3:18][NH:20][C@H:21]1[CH2:26][CH2:25][C@H:24]([CH2:27][OH:28])[CH2:23][CH2:22]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 16684438Red-AlHCID 178453972HCID 178453972、化合物

生成物 1

HCID 178484806HCID 178484806、化合物

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

反応条件

温度
105 °C

実験手順

Vitride solution (65%, 767 ml, 2.465 mol) was added dropwise over 1 h to a solution of trans-4-[(tert-butoxycarbonyl)amino]cyclohexanecarboxylic acid (commercially available, 100 g, 0.4109 mol) in toluene (1 l). After the addition was complete the reaction mixture was heated to reflux for 100-110° C. The reaction mixture was quenched with aq. Sodium sulphate solution (800 ml) at temperatures below 10° C. The reaction mixture was filtered through celite and the filter cake washed with DCM (500 ml) followed by water (100 ml). The organics layer was separated and the aqueous layer extracted twice with DCM (600 ml then 400 ml). The combined organics layers were dried over sodium sulphate and concentrated in vacuo to give the title compound (62 g).

後処理

  1. additionAfter the addition
  2. temperaturewas heated
  3. customThe reaction mixture was quenched with aq. Sodium sulphate solution (800 ml) at temperatures below 10° C
  4. filtrationThe reaction mixture was filtered through celite
  5. washthe filter cake washed with DCM (500 ml)
  6. customThe organics layer was separated
  7. extractionthe aqueous layer extracted twice with DCM (600 ml
  8. dry with materialThe combined organics layers were dried over sodium sulphate
  9. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-8df94f35bc0c4fb9a82445b56f112e86
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08987283B2

反応ノート

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