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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1707821Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1707821

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
PatentnummerUS05354913
Quelldatensatzuspto-grants-1994_10
ORD IDord-240e937eb99543268de17b1360bc38b4
Quellennotizuspto-grants-1994_10