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Hydrochloric Acid → N-(1-methylethyl)-(2-nitro-6-fluorophenyl)methylamine

HRID 583077
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HRID 583077 반응식
[N+:1]([C:4]1[CH:11]=[CH:10][CH:9]=[C:8]([F:12])[C:5]=1[CH:6]=O)([O-:3])=[O:2].[CH:13]([NH2:16])([CH3:15])[CH3:14].[BH4-].[Na+].Cl>CO>[CH3:14][CH:13]([NH:16][CH2:6][C:5]1[C:8]([F:12])=[CH:9][CH:10]=[CH:11][C:4]=1[N+:1]([O-:3])=[O:2])[CH3:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 6363IsopropylamineHCID 4311764Sodium borohydrideHCID 135240432-Fluoro-6-nitrobenzaldehyde

생성물 1

HCID 17777165N-(1-methylethyl)-(2-nitro-6-fluorophenyl)methylamine

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

To a solution of 2-nitro-6-fluorobenzaldehyde(1.21 g, 7.16 mmol) in dry methanol (15 ml), was added isopropyl amine (1 ml, 11.4 mmol) and the mixture stirred for 24 hours at room temperature in argon atmosphere. Then NaBH4 (0.3 g, 7.9 mmol) was added and the reaction mixture was stirred for 36 hours. The suspension was neutralized by addition of HCl 5N, then was extracted with diethyl ether (1×100 ml) and dried over MgSO4 and evaporated at reduced pressure to afford N-(1-methylethyl)-(2-nitro-6-fluorophenyl)methylamine as a brown oil.

후처리

  1. stirringthe reaction mixture was stirred for 36 hours
  2. extractionwas extracted with diethyl ether (1×100 ml)
  3. dry with materialdried over MgSO4
  4. customevaporated at reduced pressure

출처 및 근거

ORD 기록
ord-37b2d576b5c846d6b94415104c849d74
출처 데이터셋
uspto-grants-1999_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05929072

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