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Lithium hydroxide, monohydrate → 2-Fluoro-5-phenylamino-terephthalic Acid

HRID 970328
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HRID 970328 반응식
C[O:2][C:3](=[O:22])[C:4]1[CH:13]=[C:12]([NH:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[C:7]([C:8]([O:10]C)=[O:9])=[CH:6][C:5]=1[F:21].O.[OH-].[Li+]>CO.C1COCC1.O>[F:21][C:5]1[CH:6]=[C:7]([C:8]([OH:10])=[O:9])[C:12]([NH:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)=[CH:13][C:4]=1[C:3]([OH:22])=[O:2]
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참가 물질

6

반응물 2

HCID 168937Lithium hydroxide, monohydrateHCID 167486382-Fluoro-5-phenylamino-terephthalic Acid Dimethyl Ester

생성물 1

HCID 167483932-Fluoro-5-phenylamino-terephthalic Acid

시약·촉매·용매 3

HCID 887Methanol용매HCID 962Water용매HCID 8028Tetrahydrofuran용매

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온도
75 °C

실험 절차

A mixture of 174C (30.0 g, 9.89 mmol) and lithium hydroxide monohydrate (12.5 g, 29.7 mmol) in MeOH (200 mL), THF (200 mL) and water (100 mL) was heated at 75° C. for 0.5 h. HPLC indicated that the reaction was complete. The organic solvents were removed under reduced pressure, and the aqueous residue was diluted with water. The pH was adjusted to 3.0 with 6N aqueous hydrochloric acid which resulted in a precipitate. The solid was collected by vacuum filtration and dried under reduced pressure to provide a quantitative yeild of compound 174D as an orange-yellow solid. HPLC retention time=3.02 min. (Condition B). 1H-NMR (400 MHz, DMSO) δ7.11 (m, 1H), 7.25 (m, 2H), 7.39 (m, 2H), 7.60 (m, 1H), 7.68 (m, 1H), 9.32 (br s, 1H), and 13.55 (br s, 2H).

후처리

  1. customThe organic solvents were removed under reduced pressure
  2. additionthe aqueous residue was diluted with water
  3. customresulted in a precipitate
  4. filtrationThe solid was collected by vacuum filtration
  5. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-519e0b01bc1a47d38ac86c01f9ec3bc8
출처 데이터셋
uspto-grants-2007_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07312209B2

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