Lithium hydroxide, monohydrate → HCID 22918423, 화합물

HRID 2396045노트

반응식

HRID 2396045 반응식
C[O:2][C:3](=[O:30])[C:4]1[C:5](=[CH:10][C:11]([NH:22][C:23]2[CH:28]=[CH:27][C:26]([F:29])=[CH:25][CH:24]=2)=[C:12]([NH:14][C:15]2[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=2)[CH:13]=1)[C:6]([O:8]C)=[O:7].O.[OH-].[Li+]>CO.O>[F:21][C:18]1[CH:19]=[CH:20][C:15]([NH:14][C:12]2[CH:13]=[C:4]([C:3]([OH:30])=[O:2])[C:5](=[CH:10][C:11]=2[NH:22][C:23]2[CH:28]=[CH:27][C:26]([F:29])=[CH:25][CH:24]=2)[C:6]([OH:8])=[O:7])=[CH:16][CH:17]=1

참가 물질

5

반응물 2

HCID 168937Lithium hydroxide, monohydrateHCID 10476762HCID 10476762, 화합물

생성물 1

HCID 22918423HCID 22918423, 화합물

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매2회

실험 절차

A steady stream of argon is passed through a suspension of 5.0 g (12.12 mmol) of 4,5-bis(4-fluoroanilino)phthalic acid dimethylester in 40 ml of methanol, and a solution of 2.04 g (48.6 mmol, 2 eq) of lithium hydroxide monohydrate in 20 ml of water is added. The reaction mixture is heated to reflux for 1 hour, cooled to RT and diluted with 50 ml water. Methanol is removed by evaporation, the resulting solution is cooled to 0°, and12 ml 4N hydrochloric acid and thereafter 100 ml of water are added. After 15 min at 0°, the gray crystals are filtered off, washed with waterand resuspended twice in 100 ml toluene with removal of the toluene by distillation to yield the title compound in the form of gray crystals, FAB-MS: 385 [M+ +H].

후처리

  1. temperatureThe reaction mixture is heated
  2. temperatureto reflux for 1 hour
  3. customMethanol is removed by evaporation
  4. temperaturethe resulting solution is cooled to 0°
  5. additionand12 ml 4N hydrochloric acid and thereafter 100 ml of water are added
  6. filtrationthe gray crystals are filtered off
  7. washwashed with waterand
  8. customresuspended twice in 100 ml toluene with removal of the toluene by distillation

출처 및 근거

ORD 기록
ord-92a5aa28c08e43e8b793a231d7e81868
출처 데이터셋
uspto-grants-1996_02
특허 번호
US05491144

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