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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Water → HCID 178453954、化合物

HRID 1007291
ノート
印刷プレビュー

反応式

HRID 1007291 の反応式
[H-].[Al+3].[Li+].[H-].[H-].[H-].C[O:8][C:9]([C@H:11]1[CH2:16][CH2:15][C@@H:14]([NH:17][C:18]([O:20][C:21]([CH3:24])([CH3:23])[CH3:22])=[O:19])[CH2:13][CH2:12]1)=O.O>C(OCC)C>[C:21]([O:20][C:18]([NH:17][C@H:14]1[CH2:13][CH2:12][C@@H:11]([CH2:9][OH:8])[CH2:16][CH2:15]1)=[O:19])([CH3:24])([CH3:23])[CH3:22]
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 962WaterHCID 21226445Aluminium lithium hydride2 回HCID 178501238HCID 178501238、化合物

生成物 1

HCID 178453954HCID 178453954、化合物収率 69.7%

試薬・触媒・溶媒 1

HCID 3283Diethyl Ether溶媒2 回

実験手順

Under argon atmosphere, a suspension of 1.29 g of lithium aluminum hydride in 40 mL of anhydrous ethyl ether was treated dropwise with a solution of 5.80 g of cis-4-(tert-butoxycarbonylamino)cyclohexanecarboxylic acid methyl ester in 20 mL of anhydrous ethyl ether with cooling in ice, and stirred for 3 hours while allowing to gradually warm to room temperature. The reaction solution was cooled to 0° C., combined a small amount of water to decompose an excessive lithium aluminum hydride. The insolubles were filtered off through Celite, and the filtrate was concentrated, and then the residue was washed with n-hexane to obtain 3.60 g of the desirable compound as colorless crystals.

後処理

  1. temperaturewith cooling in ice
  2. temperatureThe reaction solution was cooled to 0° C.
  3. filtrationThe insolubles were filtered off through Celite
  4. concentrationthe filtrate was concentrated
  5. washthe residue was washed with n-hexane

出典と根拠

ORDレコード
ord-855e1c1293234cbb8c7483a5cb3e7514
出典データセット
uspto-grants-2004_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06794389B2

反応ノート

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