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1-Methylethyl 2-methoxyacetate → Methyl (1S,2S)-2-aminocyclohexane-1-carboxylate

HRID 1107671
ノート
印刷プレビュー

反応式

HRID 1107671 の反応式
[NH2:1][C@@H:2]1[CH2:7][CH2:6][CH2:5][CH2:4][C@H:3]1[C:8]([O:10][CH3:11])=[O:9].COCC(OC(C)C)=O>CC(OC)(C)C>[NH2:1][C@H:2]1[CH2:7][CH2:6][CH2:5][CH2:4][C@@H:3]1[C:8]([O:10][CH3:11])=[O:9]
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 5421921-Methylethyl 2-methoxyacetateHCID 11768827Methyl (1R,2R)-2-aminocyclohexane-1-carboxylate

生成物 1

HCID 10964775Methyl (1S,2S)-2-aminocyclohexane-1-carboxylate収率 46.7%

試薬・触媒・溶媒 1

HCID 15413tert-Butyl methyl ether溶媒

実験手順

50 g (0.32 mol) of methyl trans-2-aminocyclohexanecarboxylate were dissolved in 200 ml of MTBE and, after addition of 0.16 mol of isopropyl methoxyacetate and 0.5 g of Novozym 435 (Novo Nordisk), shaken at room temperature for 8 h. The enzyme was filtered off and then the solvent was removed and the residue was distilled under reduced pressure. 23.5 g of methyl (1S,2S)-2-aminocyclohexanecarboxylate and 35.2 g of methyl (1R,2R)-2-(2-methoxyacetylamino) cyclohexanecarboxylate were obtained, each with an ee of 99.8%. The ee of the amine was determined after N-acylation with acetic anhydride by gas chromatography on a B-PH GC column (supplied by Astec, N.J., USA), while the N-2-methoxyacetamide was put on this column without derivatization.

後処理

  1. filtrationThe enzyme was filtered off
  2. customthe solvent was removed
  3. distillationthe residue was distilled under reduced pressure

出典と根拠

ORDレコード
ord-d5754a2c731c4a1ab2b3cc74f5e8a928
出典データセット
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06063615

反応ノート

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