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Sulfuric Acid → HCID 54569995, 화합물

HRID 257330
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HRID 257330 반응식
[C:1]([O:4][C:5](=O)[CH3:6])(=[O:3])[CH3:2].S(=O)(=O)(O)O.[CH3:13][O:14][C:15]([C:17]1([F:23])CC[CH2:19][CH:18]1O)=[O:16]>>[CH3:13][O:14][C:15]([C:17]1([F:23])[CH2:18][CH2:19][CH2:6][CH:5]1[O:4][C:1](=[O:3])[CH3:2])=[O:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 1118Sulfuric AcidHCID 7918Acetic AnhydrideHCID 19783080HCID 19783080, 화합물

생성물 1

HCID 54569995HCID 54569995, 화합물수율 73.5%

실험 절차

0.32 g (3 mmol) of acetic anhydride and a catalytic amount of concentrated sulfuric acid were added at room temperature to 0.5 g (3 mmol) of 1-fluoro-2-hydroxycyclopentanecarboxylic acid methyl ester in cis form (compound number 2a) synthesized in Example 1, and the mixture was stirred for 5 hours. The reaction solution was poured into ice water and extracted with ethyl acetate, and the extract was successively washed with saturated saline, a saturated aqueous sodium bicarbonate solution and saturated saline. The ethyl acetate layer was dried over anhydrous magnesium sulfate and the solvent was distilled away to obtain 0.45 g (yield: 72%) of the objective 2-acetoxy-1-fluoro-1-cyclopentanecarboxylic acid methyl ester in cis form (compound number 3a).

후처리

  1. customsynthesized in Example 1
  2. extractionextracted with ethyl acetate
  3. washthe extract was successively washed with saturated saline
  4. dry with materialThe ethyl acetate layer was dried over anhydrous magnesium sulfate
  5. distillationthe solvent was distilled away

출처 및 근거

ORD 기록
ord-be02a21cd978486d86de4bdc35b9eabb
출처 데이터셋
uspto-grants-1993_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05262385

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