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Acetic Acid → 2-Amino-4-fluoro-6-methylbenzonitrile

HRID 17549
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HRID 17549 반응식
C(O)(=O)C.Cl.O.O.[Sn](Cl)(Cl)(Cl)Cl.[F:13][C:14]1[CH:21]=[C:20]([N+:22]([O-])=O)[C:17]([C:18]#[N:19])=[C:16]([CH3:25])[CH:15]=1.[OH-].[Na+]>CO>[NH2:22][C:20]1[CH:21]=[C:14]([F:13])[CH:15]=[C:16]([CH3:25])[C:17]=1[C:18]#[N:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 176Acetic AcidHCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 544206034-Fluoro-2-methyl-6-nitrobenzonitrileHCID 85782573Tin tetrachloride dihydrate

생성물 1

HCID 450790392-Amino-4-fluoro-6-methylbenzonitrile수율 104.9%

시약·촉매·용매 1

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 887Methanol용매

실험 절차

Acetic acid (16.0 ml, 28 mmol) was added to a concentrated hydrochloric acid (90 ml) solution of tin chloride dihydrate (63.1 g, 280 mmol), and 4-fluoro-2-methyl-6-nitrobenzonitrile (I-263) (16.8 g, 93.3 mmol) was added, then methanol (8 ml) was added. Since the reaction liquid greatly generated heat, it was cooled with ice. After stirring for 1 hour, the reaction mixture liquid was poured into aqueous sodium hydroxide solution (4.6 M, 500 ml) with ice therein. The precipitated solid was collected by filtration, washed with water, then dried to obtain the entitled compound (14.7 g, 99%) as a gray solid.

후처리

  1. additionwas added
  2. customSince the reaction liquid
  3. temperaturegreatly generated heat
  4. temperatureit was cooled with ice
  5. filtrationThe precipitated solid was collected by filtration
  6. washwashed with water
  7. customdried

출처 및 근거

ORD 기록
ord-234628892ac14dcf83801d1683fe9b29
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07737166B2

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