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Sulfuric Acid → Sodium

HRID 1027336
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HRID 1027336 반응식
[Na:1].[F:2][C:3]([F:11])([S:7]([OH:10])(=[O:9])=[O:8])[C:4]([OH:6])=[O:5].[O:12]=[C:13]1[CH:20]2[CH2:21][C:16]3(O)[CH2:17][CH:18]([CH2:22][CH:14]1[CH2:15]3)[CH2:19]2.C(C1C=CC=CC=1)C.S(=O)(=O)(O)O>>[Na:1].[F:2][C:3]([F:11])([S:7]([OH:10])(=[O:9])=[O:8])[C:4]([O:6][C:18]12[CH2:22][CH:14]3[CH2:15][CH:16]([CH2:21][CH:20]([C:13]3=[O:12])[CH2:19]1)[CH2:17]2)=[O:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 5

HCID 1118Sulfuric AcidHCID 7500EthylbenzeneHCID 64184IdramantoneHCID 6547892,2-Difluoro-2-sulfoacetic acidHCID 5360545Sodium

생성물 2

HCID 5360545SodiumHCID 21111910HCID 21111910, 화합물

실험 절차

To a mixture of 5.0 parts of sodium salt of difluorosulfoacetic acid (purity: 62.6%), 2.6 parts of 4-oxo-1-adamantanol and 100 parts of ethylbenzene, 0.6 part of concentrated sulfuric acid was added and the resultant solution was refluxed for 30 hours. The mixture was cooled and filtrated. The obtained solid was washed with tert-butyl methyl ether to obtain 5.5 parts of sodium salt of 4-oxo-1-adamantyl difluorosulfoacetate. The purity thereof was 35.6% according to 1H-NMR analysis.

후처리

  1. additionwas added
  2. temperatureThe mixture was cooled
  3. filtrationfiltrated
  4. washThe obtained solid was washed with tert-butyl methyl ether

출처 및 근거

ORD 기록
ord-daa6445445b24ee8ac4fcb6f015a5123
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08735044B2

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