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Formic Acid → n-(4-Iodophenyl)formamide

HRID 30830
ノート
印刷プレビュー

反応式

HRID 30830 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 3

HCID 284Formic AcidHCID 7918Acetic AnhydrideHCID 108934-Iodoaniline

生成物 1

HCID 291922n-(4-Iodophenyl)formamide収率 99%

試薬・触媒・溶媒 4

HCID 962Water溶媒HCID 1140Toluene溶媒
HCID 8028
Tetrahydrofuran
溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

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=2Hz, 1H), 7.64 (d, J=12Hz, 2H), 7.40 (d, J=11.7 Hz, 2H) and 30% tautomer; ESI-MS m/z 248.0 (MH+).

後処理

  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

出典と根拠

ORDレコード
ord-0bfa51b761354dab84aad1e5890e9095
出典データセット
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07423156B2

反応ノート

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