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Iodine → 5-Bromonaphthalene-2-carboxylic acid

HRID 2221289
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HRID 2221289 반응식
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:11]([OH:13])=[O:12].[Br:14]Br.II>C(O)(=O)C>[Br:14][C:6]1[CH:7]=[CH:8][CH:9]=[C:10]2[C:5]=1[CH:4]=[CH:3][C:2]([C:11]([OH:13])=[O:12])=[CH:1]2
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참가 물질

5

반응물 3

HCID 807IodineHCID 71232-Naphthoic acidHCID 24408Bromine

생성물 1

HCID 149606465-Bromonaphthalene-2-carboxylic acid수율 53.4%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

To a boiling solution of 2-naphthoic acid (10.00 g, 58.14 mmol) in acetic acid (50 mL) is added dropwise bromine (3 mL) containing iodine (0.25 g). After the addition is complete, the solution is refluxed for 0.5 hr. A white precipitate forms during cooling and is isolated by filtration, washed with acetic acid and then water. The solid is triturated in methanol (100 mL) and 7.01 g (53.4% yield) of the desired product is obtained as a white solid. m.p. 248-250° C. 1H NMR (300 MHz, CD3OD): δ 8.94 (d, J=1.8 Hz, 1H), 8.52-8.42 (m, 3H), 8.27 (dd, J=1.8, 7.5 Hz, 1H), 7.79 (t, J=8.4 Hz, 1H).

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후처리

  1. additionAfter the addition
  2. temperaturethe solution is refluxed for 0.5 hr
  3. temperatureA white precipitate forms during cooling
  4. customis isolated by filtration
  5. washwashed with acetic acid
  6. customThe solid is triturated in methanol (100 mL)

출처 및 근거

ORD 기록
ord-49889830defc4e909a60fd35f4a4cc42
출처 데이터셋
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07368462B1

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