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Tetrahydrofuran → 2,4-Difluoro-5-sulfobenzoic acid

HRID 1992156
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HRID 1992156 반응식
[BH4-].[Na+].Cl[S:4]([C:7]1[C:8]([F:17])=[CH:9][C:10]([F:16])=[C:11]([CH:15]=1)[C:12]([OH:14])=[O:13])(=[O:6])=[O:5].C1C[O:21]CC1>>[F:16][C:10]1[CH:9]=[C:8]([F:17])[C:7]([S:4]([OH:21])(=[O:6])=[O:5])=[CH:15][C:11]=1[C:12]([OH:14])=[O:13]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 8028TetrahydrofuranHCID 4311764Sodium borohydrideHCID 107535965-(Chlorosulfonyl)-2,4-difluorobenzoic acid

생성물 1

HCID 587279372,4-Difluoro-5-sulfobenzoic acid수율 100%

실험 절차

Sodium borohydride (0.59 g, 15.6 mmol, 8 equiv) was added portionwise to a solution of 5-(chlorosulfonyl)-2,4-difluorobenzoic acid 885-6a (0.5 g, 1.9 mmol, 1 equiv) in 10 mL THF at 0° C. The reaction was stirred at this temperature for 1 h and then concentrated down and the residue acidified to pH 2 with 5N HCl. The precipitate was removed by filtration and the liquid concentrated down to provide 2,4-difluoro-5-sulfobenzoic acid 885-6b as a white solid (433 mg, 100% yield)

후처리

  1. concentrationconcentrated down
  2. customThe precipitate was removed by filtration
  3. concentrationthe liquid concentrated down

출처 및 근거

ORD 기록
ord-f08651a63b354b6c8b3ed5d43fe6b90f
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07645771B2

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