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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107671Generated: November 1, 2026

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

https://huagongshe.com/reaction/1107671

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methylethyl 2-methoxyacetateHCID 542192—
ReactantMethyl (1R,2R)-2-aminocyclohexane-1-carboxylateHCID 11768827—
Solventtert-Butyl methyl etherHCID 15413—
ProductMethyl (1S,2S)-2-aminocyclohexane-1-carboxylateHCID 1096477546.7%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06063615
Source datasetuspto-grants-2000_05
ORD IDord-d5754a2c731c4a1ab2b3cc74f5e8a928
Source noteuspto-grants-2000_05