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Hydrochloric Acid → Methyl 6-fluorochromane-4-carboxylate

HRID 487204
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HRID 487204 반응식
[F:1][C:2]1[CH:3]=[CH:4][C:5]2[O:10][CH2:9][CH2:8][CH:7]([C:11]([OH:13])=[O:12])[C:6]=2[CH:14]=1.Cl.[CH3:16]O>>[F:1][C:2]1[CH:3]=[CH:4][C:5]2[O:10][CH2:9][CH2:8][CH:7]([C:11]([O:13][CH3:16])=[O:12])[C:6]=2[CH:14]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 313Hydrochloric AcidHCID 887MethanolHCID 139537996-Fluoro-3,4-dihydro-2H-1-benzopyran-4-carboxylic acid

생성물 1

HCID 14986536Methyl 6-fluorochromane-4-carboxylate

실험 절차

A solution of 8.4 g of the 6-fluoro-2,3-dihydro-4H-benzopyran-4-carboxylic acid in 580 mL of methanol was perfused with HCl gas for 5 minutes. The resulting solution was stirred at room temperature overnight. The volatiles were evaporated and the residue dissolved in ether. The ether layer was washed with water then dried over Na2SO4, filtered and evaporated to give 8.7 g of crude product which was purified by chromatography on 300 g of silica gel eluting with CH2Cl2 to give 6.2 g of product as an oil. NMR (CDCl3) ppm (delta): 2.00-2.40 (m, 2H), 3.80 (s, 3H), 2.5 (t, 1H, J=4 Hz), 7.10-6.70 (m, 3H).

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  • customThe volatiles were evaporated
  • dissolutionthe residue dissolved in ether
  • washThe ether layer was washed with water
  • dry with materialthen dried over Na2SO4
  • filtrationfiltered
  • customevaporated
  • customto give 8.7 g of crude product which
  • customwas purified by chromatography on 300 g of silica gel eluting with CH2Cl2
  • 출처 및 근거

    ORD 기록
    ord-6359c97b87d6493d8935d9159bb10cc5
    출처 데이터셋
    uspto-grants-1994_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05294635

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