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

HRID 1107671
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HRID 1107671 반응식
[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]
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참가 물질

4

반응물 2

HCID 5421921-Methylethyl 2-methoxyacetateHCID 11768827Methyl (1R,2R)-2-aminocyclohexane-1-carboxylate

생성물 1

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

시약·촉매·용매 1

HCID 15413tert-Butyl methyl ether용매

실험 절차

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.

후처리

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

출처 및 근거

ORD 기록
ord-d5754a2c731c4a1ab2b3cc74f5e8a928
출처 데이터셋
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06063615

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