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Trifluoroacetic acid → 2-Bromo-5-methoxy-3-methyl-phenylamine

HRID 723167
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HRID 723167 반응식
C(OC(=O)[NH:7][C:8]1[CH:13]=[C:12]([O:14][CH3:15])[CH:11]=[C:10]([CH3:16])[C:9]=1[Br:17])(C)(C)C.FC(F)(F)C(O)=O>C(Cl)Cl>[Br:17][C:9]1[C:10]([CH3:16])=[CH:11][C:12]([O:14][CH3:15])=[CH:13][C:8]=1[NH2:7]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 69586528(2-Bromo-5-methoxy-3-methyl-phenyl)-carbamic acid tert-butyl ester

생성물 1

HCID 218864892-Bromo-5-methoxy-3-methyl-phenylamine수율 99.5%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of (2-bromo-5-methoxy-3-methyl-phenyl)-carbamic acid tert-butyl ester ((Example 198: step b) 3.00 g, 9.49 mmol) in CH2Cl2 (50 mL) was treated with trifluoroacetic acid (7.00 mL) dropwise. The solution was stirred at room temperature 1.3 h. The solvents were evaporated in vacuo to yield the product 2-bromo-5-methoxy-3-methyl-phenylamine (2.04 g, 65%) as a yellow solid trifluoroacetate salt. The crude mixture was used directly in the next reaction.

후처리

  1. customThe solvents were evaporated in vacuo

출처 및 근거

ORD 기록
ord-1c72fc08296a4b249e37c73ba120fbb1
출처 데이터셋
uspto-grants-2006_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07138530B2

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