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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Pivaloyl chloride → 4-bromo-2,6-dichloro-N-pivaloylaniline

HRID 1736242
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HRID 1736242 반응식
Cl.[Br:2][C:3]1[CH:9]=[C:8]([Cl:10])[C:6]([NH2:7])=[C:5]([Cl:11])[CH:4]=1.[C:12](Cl)(=[O:17])[C:13]([CH3:16])([CH3:15])[CH3:14]>N1C=CC=CC=1>[Br:2][C:3]1[CH:9]=[C:8]([Cl:10])[C:6]([NH:7][C:12](=[O:17])[C:13]([CH3:16])([CH3:15])[CH3:14])=[C:5]([Cl:11])[CH:4]=1
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참가 물질

4

반응물 2

HCID 62493Pivaloyl chlorideHCID 194349524-Bromo-2,6-dichloroaniline hydrochloride

생성물 1

HCID 194349714-bromo-2,6-dichloro-N-pivaloylaniline수율 97%

시약·촉매·용매 1

HCID 1049Pyridine용매

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온도
40 °C

실험 절차

12.0 g (50.0 mmol) of 4-bromo-2,6-dichloroaniline hydrochloride was dissolved in 50 mL of pyridine, 9.90 mL (80.0 mmol) of pivaloyl chloride and 0.61 g (5.0 mmol) of N,N-dimethylaminopyridine were added and the mixture was stirred at 40° C. for 28 hours. Thereafter, substantially the same manner as that in Reference Example (1) was repeated to give 15.7 g of 4-bromo-2,6-dichloro-N-pivaloylaniline (yield: 97%).

출처 및 근거

ORD 기록
ord-a263e0617b6d4bc99550e0abe3446c07
출처 데이터셋
uspto-grants-1996_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05539112

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