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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethyl 2-aminocyclohex-1-ene-1-carboxylate → (1S,2R)-ethyl 2-benzoylaminocyclohexane-1-carboxylate

HRID 592114
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인쇄 미리보기

반응식

HRID 592114 반응식
[NH2:1][C:2]1[CH2:7][CH2:6][CH2:5][CH2:4][C:3]=1[C:8]([O:10][CH2:11][CH3:12])=[O:9].[H][H]>CO>[C:8]([NH:1][C@@H:2]1[CH2:7][CH2:6][CH2:5][CH2:4][C@@H:3]1[C:8]([O:10][CH2:11][CH3:12])=[O:9])(=[O:9])[C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][CH:2]=1
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참가 물질

4

반응물 2

HCID 312929Ethyl 2-aminocyclohex-1-ene-1-carboxylateHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 92139654(1S,2R)-ethyl 2-benzoylaminocyclohexane-1-carboxylate

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
25 °C

실험 절차

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.

후처리

  1. customfor organic synthesis (2.5 ml)
  2. customAfter completion of the reaction

출처 및 근거

ORD 기록
ord-2793a6c70d324ce5bb242dd662902695
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09238667B2

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