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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 37728Erstellt: 24. Oktober 2026

Methanol → methyl (S)-7-(4-fluorophenyl)-7-hydroxyheptanoate

https://huagongshe.com/de/reaction/37728

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
Edukt(R)-2-Methyl-CBS-oxazaborolidineHCID 9838490—
EduktMethyl 7-(4-fluorophenyl)-7-oxoheptanoateHCID 19936161—
LösungsmittelTetrahydrofuranHCID 8028—
Produktmethyl (S)-7-(4-fluorophenyl)-7-hydroxyheptanoateHCID 1056289298,4%

Reaktionsschritte

To a solution of (R)-3,3-diphenyl-1-methyltetrahydro-1H,3H-pyrrolo[1,2-c] [1,3,2]oxazaborole (1.1 g) in tetrahydrofuran (20 ml) was added at 0° C. 1M tetrahydrofuran solution of boranetetrahydrofuran complex (4 ml). To this solution were added dropwise a solution of methyl 7-(4-fluorophenyl)-7-oxoheptanoate (10.0 g, 39.6 mmol) in tetrahydrofuran (20 ml) and 1M tetrahydrofuran solution of boranetetrahydrofuran complex (20 ml), simultaneously, taking 25 minutes. The mixture was stirred for 30 minutes at the same temperature range, to which was added methanol (20 ml), followed by stirring for 30 minutes at room temperature. The solvent was distilled off under reduced pressure, and the residue was subjected to a silica gel column chromatography to give methyl (S)-7-(4-fluorophenyl)-7-hydroxyheptanoate (9.91 g). Physico-chemical properties and spectral data of this product are shown in [Table 7]. Likewise, Compound 1-2 was prepared.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05420363
Quelldatensatzuspto-grants-1995_05
ORD IDord-5fdb7b29cd3c48a78d22172e09f3d335
Quellennotizuspto-grants-1995_05