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Formic Acid → n-(4-Iodophenyl)formamide

HRID 9518
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HRID 9518 반응식
[I:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][CH:3]=1.[C:9](OC(=O)C)(=[O:11])C.C(O)=O>C1COCC1.C1(C)C=CC=CC=1.O.C(OCC)(=O)C>[CH:4]1[C:5]([NH:6][CH:9]=[O:11])=[CH:7][CH:8]=[C:2]([I:1])[CH:3]=1
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참가 물질

8

반응물 3

HCID 284Formic AcidHCID 7918Acetic AnhydrideHCID 108934-Iodoaniline

생성물 1

HCID 291922n-(4-Iodophenyl)formamide수율 99%

시약·촉매·용매 4

HCID 962Water용매HCID 1140Toluene용매
HCID 8028
Tetrahydrofuran
용매
HCID 8857Ethyl Acetate용매

실험 절차

To a solution of 4-iodoaniline (30.0 g, 137 mmol) in 100 mL THF and 100 mL toluene, a solution of acetic anhydride (16.0 g, 157 mmol) and formic acid (10.8 g, 235 mmol) was slowly added from an addition funnel under argon atmosphere. The reaction mixture temperature was maintained below 15° C. during the addition. After the addition was finished, the reaction mixture was stirred at rt overnight. The reaction mixture was diluted with water (300 mL) and ethyl acetate (200 mL). The organic layer was separated, washed with water (2×200 mL), and 200 mL saturated aqueous sodium bicarbonate solution. After drying over sodium sulfate, the mixture was concentrated under reduced pressure to afford 4-Iodoformanilide as an off-white solid (33.5 g, >98%). 1H NMR (DMSO-d6) δ 10.27 (s, 1H), 8.26 (d, J=2 Hz, 1H), 7.64 (d, J=12 Hz, 2H), 7.40 (d, J=11.7 Hz, 2H) and 30% tautomer; ESI-MS m/z 248.0 (MH+).

후처리

  1. temperatureThe reaction mixture temperature was maintained below 15° C. during the addition
  2. additionAfter the addition
  3. customThe organic layer was separated
  4. washwashed with water (2×200 mL), and 200 mL saturated aqueous sodium bicarbonate solution
  5. dry with materialAfter drying over sodium sulfate
  6. concentrationthe mixture was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-3117c94e8c2e4eec9d869a0c62704a73
출처 데이터셋
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07091228B2

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