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Ethyl Acetate → D-Alloisoleucine, methyl ester

HRID 2408430
ノート
印刷プレビュー

反応式

HRID 2408430 の反応式
Cl.[NH2:2][C@@H:3]([C:8]([O:10][CH3:11])=[O:9])[C@H:4]([CH2:6][CH3:7])[CH3:5].C(OCC)(=O)C.C(=O)([O-])[O-].[K+].[K+]>O>[NH2:2][C@@H:3]([C:8]([O:10][CH3:11])=[O:9])[C@H:4]([CH2:6][CH3:7])[CH3:5]
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 8857Ethyl AcetateHCID 11430Potassium CarbonateHCID 12890355D-Alloisoleucine, methyl ester, hydrochloride (1:1)2 回

生成物 1

HCID 6950463D-Alloisoleucine, methyl ester

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Methyl d-alloisoleucinate hydrochloride (Compound 2) was charged to ethyl acetate. A solution of potassium carbonate in water was then added. The mixture was then stirred vigorously at room temperature for 1 hour. The two layers were separated and the aqueous layer further extracted with ethyl acetate. The organic layers were combined and washed with brine. The organic layers were then concentrated in vacuo and filtered to yield methyl D-alloisoleucinate (Compound 3) as a pale yellow oil.

後処理

  1. customThe two layers were separated
  2. extractionthe aqueous layer further extracted with ethyl acetate
  3. washwashed with brine
  4. concentrationThe organic layers were then concentrated in vacuo
  5. filtrationfiltered

出典と根拠

ORDレコード
ord-847d661b01ab47c6a51ffa0babd7c4b3
出典データセット
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08815856B2

反応ノート

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