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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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1-(Aminomethyl)cyclohexan-1-ol → 1-Oxa-3-azaspiro(4.5)decan-2-one

HRID 1180575
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인쇄 미리보기

반응식

HRID 1180575 반응식
[NH2:1][CH2:2][C:3]1([OH:9])[CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1.[C:10]([O:14]C(OC(OC(C)(C)C)=O)=O)(C)(C)C>CN(C)C1C=CN=CC=1.C(#N)C.C(O)(=O)C.Cl>[O:9]1[C:3]2([CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]2)[CH2:2][NH:1][C:10]1=[O:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 2

HCID 776141-(Aminomethyl)cyclohexan-1-olHCID 90495Di-tert-butyl dicarbonate

생성물 1

HCID 3490431-Oxa-3-azaspiro(4.5)decan-2-one

시약·촉매·용매 4

HCID 142844-(Dimethylamino)pyridine촉매HCID 176Acetic Acid용매HCID 313Hydrochloric Acid용매HCID 6342Acetonitrile용매

실험 절차

0.65 g (5.0 mmol) of 1-(aminomethyl)-cyclohexanol, 1.2 g (5.5 mmol) di-tert.-butyldicarbonate ((Boc)2O) and 0.611 g 4-dimethylaminopyridine were dissolved in 50 ml acetonitrile and agitated overnight at room temperature. The mixture was then fully turned over, the residue was dissolved in 20 ml acetic acid and again turned over. The residue was taken up in 25 ml 1 M hydrochloric acid and extracted with 50 ml toluene.

후처리

  1. extractionextracted with 50 ml toluene

출처 및 근거

ORD 기록
ord-7ac8cd96d6e54722932bd77cad796e30
출처 데이터셋
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07282515B2

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