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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethoxalyl chloride → Ethyl[(3,3-dimethyl-2-oxobutyl)amino](oxo)acetate

HRID 1748327
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인쇄 미리보기

반응식

HRID 1748327 반응식
Cl.[NH2:2][CH2:3][C:4](=[O:9])[C:5]([CH3:8])([CH3:7])[CH3:6].C(N(CC)C(C)C)(C)C.Cl[C:20](=[O:26])[C:21]([O:23][CH2:24][CH3:25])=[O:22]>C(Cl)Cl>[CH2:24]([O:23][C:21](=[O:22])[C:20]([NH:2][CH2:3][C:4](=[O:9])[C:5]([CH3:8])([CH3:7])[CH3:6])=[O:26])[CH3:25]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 20884Ethoxalyl chlorideHCID 81531DiisopropylethylamineHCID 221479671-Amino-3,3-dimethylbutan-2-one hydrochloride

생성물 1

HCID 11241370Ethyl[(3,3-dimethyl-2-oxobutyl)amino](oxo)acetate수율 81%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

To a mixture of 1-amino-3,3-dimethylbutan-2-one hydrochloride salt (35 g, 231 mmol) in CH2Cl2 (500 mL) at 0° C. are added N,N-diisopropylethylamine (74 g, 577 mmol) and ethyl chloro(oxo)acetate (31.5 g, 231 mmol) slowly over a period of 15 min. The reaction mixture is stirred at room temperature for 2 h and is filtered through Celite. The filtrate is concentrated to afford the title compound (40 g, 81%).

후처리

  1. filtrationis filtered through Celite
  2. concentrationThe filtrate is concentrated

출처 및 근거

ORD 기록
ord-12fcdcfefc2e4f7b886a1a5705332ca9
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09150577B2

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