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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Trimethylsilyldiazomethane → Methyl 4-amino-3-bromo-5-nitrobenzoate

HRID 592318
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HRID 592318 반응식
[NH2:1][C:2]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][C:3]=1[Br:14].[CH3:15][Si](C=[N+]=[N-])(C)C>ClCCl.CO>[NH2:1][C:2]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][C:5]([C:6]([O:8][CH3:15])=[O:7])=[CH:4][C:3]=1[Br:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 167693TrimethylsilyldiazomethaneHCID 547587704-Amino-3-bromo-5-nitrobenzoic acid

생성물 1

HCID 13685347Methyl 4-amino-3-bromo-5-nitrobenzoate수율 40%

시약·촉매·용매 2

HCID 887Methanol용매HCID 6344Dichloromethane용매

실험 절차

To a solution of 4-amino-3-bromo-5-nitrobenzoic acid (3.65 g, 14.0 mmol) in dichloromethane (35 mL) and methanol (35 mL) at 0° C. was slowly added trimethylsilyl-diazomethane (8.74 mL, 17.5 mmol). The mixture was allowed to warm to ambient temperature and concentrated. Purification by silica gel chromatography (100% hexanes→50% hexanes/ethyl acetate) gave the title compound (1.54 g). LC-MS [M]=275.1.

후처리

  1. customat 0° C.
  2. concentrationconcentrated
  3. customPurification by silica gel chromatography (100% hexanes→50% hexanes/ethyl acetate)

출처 및 근거

ORD 기록
ord-4f3a9c84fc614cf98f51713fec7f35d5
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09238647B2

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