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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592114Generated: October 30, 2026

Ethyl 2-aminocyclohex-1-ene-1-carboxylate → (1S,2R)-ethyl 2-benzoylaminocyclohexane-1-carboxylate

https://huagongshe.com/reaction/592114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-aminocyclohex-1-ene-1-carboxylateHCID 312929—
ReactantHCID 178418361HCID 178418361—
SolventMethanolHCID 887—
Product(1S,2R)-ethyl 2-benzoylaminocyclohexane-1-carboxylateHCID 92139654—

Reaction Conditions

Temperature25 °C

Reaction Steps

In a 10 mL test tube were charged diacetato{(S)-2,2′-bis[bis(3,5-di-tert-butyl-4-methoxyphenyl)phosphino]-1,1′-binaphthyl}ruthenium (II) (12.9 mg), and ethyl 2-aminocyclohexene-1-carboxylate (50 mg), and the mixture was set on a pressurization apparatus. Argon substitution was performed, and dehydrated methanol for organic synthesis (2.5 ml) was injected with pressure. Thereafter, hydrogen (1 MPa) was charged in and the mixture was stirred at 25° C. for 18 hr. After completion of the reaction, the reaction mixture was analyzed by HPLC.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238667B2
Source datasetuspto-grants-2016_01
ORD IDord-2793a6c70d324ce5bb242dd662902695
Source noteuspto-grants-2016_01