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Hydrochloric Acid → 6-Amino-5-bromobenzofuran-3-carboxylic acid

HRID 595535
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HRID 595535 반응식
[NH2:1][C:2]1[C:15]([Br:16])=[CH:14][C:5]2[C:6]([C:9]([O:11]CC)=[O:10])=[CH:7][O:8][C:4]=2[CH:3]=1.O[Li].O.Cl>O1CCOCC1.O>[NH2:1][C:2]1[C:15]([Br:16])=[CH:14][C:5]2[C:6]([C:9]([OH:11])=[O:10])=[CH:7][O:8][C:4]=2[CH:3]=1
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참가 물질

6

반응물 3

HCID 313Hydrochloric AcidHCID 168937Lithium hydroxide, monohydrateHCID 89428742Ethyl 6-amino-5-bromobenzofuran-3-carboxylate

생성물 1

HCID 903324196-Amino-5-bromobenzofuran-3-carboxylic acid수율 97.6%

시약·촉매·용매 2

HCID 962Water용매2회HCID 312751,4-Dioxane용매

실험 절차

To a solution of the compound ethyl 6-amino-5-bromobenzofuran-3-carboxylate (58 g, 204 mmol) in 1,4-dioxane and H2O (850 mL and 150 mL) was added LiOH.H2O (42.8 g, 1.02 mol). The reaction mixture was refluxed for 2 hours, and then 400 mL H2O was added to the reaction mixture. After acidifying to pH 4˜5 with HCl, the resulting solid was filtered to give 6-amino-5-bromobenzofuran-3-carboxylic acid (51 g, yield: 97%). 1H-NMR (400 MHz, DMSO-d6) δ 8.36 (s, 1H), 7.87 (s, 1H), 7.02 (s, 1H), 5.51 (br s, 2H).

후처리

  1. temperatureThe reaction mixture was refluxed for 2 hours
  2. filtrationthe resulting solid was filtered

출처 및 근거

ORD 기록
ord-2dc06e2f60454f269264f39842de89c5
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09242998B2

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