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Hydrochloric Acid → Methyl 6-fluorochromane-4-carboxylate

HRID 2248283
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2248283
[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
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

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

Produkt 1

HCID 14986536Methyl 6-fluorochromane-4-carboxylate

Versuchsvorschrift

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).

Aufarbeitung

  1. customThe volatiles were evaporated
  2. dissolutionthe residue dissolved in ether
  3. washThe ether layer was washed with water
  4. dry with materialthen dried over Na2SO4
  5. filtrationfiltered
  6. customevaporated
  7. customto give 8.7 g of crude product which
  8. customwas purified by chromatography on 300 g of silica gel eluting with CH2Cl2

Quellen und Nachweise

ORD-Eintrag
ord-12eca53ae4b84a6fa20480de0c74d0d5
Quelldatensatz
uspto-grants-1991_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05039672

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